Evonik Evonik

X
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
  • A company that focuses on trading of various pharmaceutical products is looking for suppliers of Ephedrine HCl API for commercial purposes. The suppliers must support this enquiry with CoA.
    10 May 2024
    A company that focuses on distribution of various pharmaceutical products is looking for suppliers of Ergocriptine (5 kg) API for commercial purposes. The suppliers must support this enquiry with CoA.
    10 May 2024

    Comment Comment

    Reply text-arrow

  • A company that focuses on development, manufacturing and distribution of various finished formulations is looking for suppliers of USP/EP/BP Polyquaternium-1 (100 g) API for development purposes. The suppliers must support this enquiry with USDMF, GMP & CoA.
    09 May 2024
    A company that focuses on research, development & manufacturing of oral solid, parenteral and topical finished formulations is looking for suppliers of Avibactam Sodium (2 kg) API for both development purposes. The suppliers must support this enquiry with DMF & CoA.
    09 May 2024
  • A company that focuses on manufacturing and distribution of various finished formulations is looking for suppliers of Calcium Sennoside (2 kg) API for development purposes. The suppliers must support this enquiry with CoA.
    09 May 2024
    A firm specializing in the synthesis of a diverse array of organic compounds to meet the requirements of both pharmaceutical and chemical sectors is looking for suppliers of Cefditoren (1 kg) API for development purposes. The suppliers must support this enquiry with CoA.
    09 May 2024

    Comment Comment

    Reply text-arrow

  • A large pharmaceutical company based in India that devotes itself to R&D, production, marketing and sales of active pharmaceutical ingredients and pharmaceutical intermediates is looking for suppliers of Various Finished Formulations for commercial purposes. The required quantity is MOQ. The supplier must support this enquiry with EU GMP & Serialization availability.
    1. Dapagliflozin (5 mg) + Metformin (1000 mg) IR Tablets
    2. Dapagliflozin (5 mg) + Metformin (850 mg) IR Tablets
    06 May 2024
    A company that focuses on manufacturing and distribution of various finished formulations used in surgery, dermatology, orthopedics, pediatrics, cardiology, gynecology, therapy and other areas of modern medicine is looking for suppliers of Gynanfort suppositories for commercial purposes. The required quantity is 30,000 packs for first year. The supplier must support this enquiry with GMP, ISO & e-CTD dossier.
    26 Apr 2024
  • A large pharmaceutical company that devotes itself to R&D, production, marketing and sales of active pharmaceutical ingredients and pharmaceutical intermediates is looking for suppliers of Citicoline (1g/ dose) Sachet- 10 ml pack for commercial purposes. The required quantity is MOQ. The supplier must support this enquiry with EAEU.
    18 Apr 2024
    A company that focuses on manufacturing and distribution of various finished formulations used in surgery, dermatology, orthopedics, pediatrics, cardiology, gynecology, therapy and other areas of modern medicine is looking for suppliers of various finished formulation for commercial purposes. The required quantity is 10,000 packs.
    1. Clindamycin 100 mg + Clotrimazole 200 mg suppositories.
    2. Clindamycin 100 mg + Clotrimazole 100 mg + Tinidazole 100 mg suppositories.
    3. Metronidazole 500 mg + Neomycin sulfate 65 000 IU + Nystatin 100 000 IU suppositories.
    4. Neomycin 83 mg + Metronidazole 500 mg + Clotrimazole 100 mg suppositories.
    5. Metamizole 400 mg + Drotaverine hydrochloride 40 mg + Caffeine 60 mg Tablets.
    6. Ibuprofen 400 mg + Drotaverine hydrochloride 80 mg Tablets.
    7. Drotaverine 80 mg + Paracetamol 500 mg Tablets.
    8. Drotaverine 80 mg + Mefenamic acid 250 mg Tablets.
    9. Dicycloverine 10 mg + Mefenamic acid 250 mg Tablets.
    10. Dicycloverine 20 mg + Paracetamol 500 mg + Mefenamic acid 250 mg Tablets.
    11. Orphenadrine citrate 35 mg + Mefenamic acid 250 mg Tablets.
    12. Orphenadrine citrate 50 mg + Aspirin 770 mg + Caffeine 60 mg Tablets.
    13. Hyoscine butylbromide 10 mg + Ketoprofen 100 mg Tablets.
    14. Hyoscine butylbromide 20 mg + Ibuprofen 400 mg + Caffeine 50 mg Tablets.
    15. Hyoscine butylbromide 20 mg + Ibuprofen 400 mg Tablets.
    16. Hyoscine butylbromide 10 mg + Metamizole 250 mg Tablets.
    17. Hyoscine butylbromide 10 mg + Paracetamol 500 mg Tablets.
    16 Apr 2024
  • A company that provides a range of full R&D pharmaceutical services and drug delivery solutions is looking for GMP & EMEA/ USFDA Certified CDMO to manufacture powders & granules. The required packaging is PET-glass bottle/ sachet stick pack. The country of distribution is Europe & United States. The geographical preference for service provider is Canada, EMEA & United States.
    19 Apr 2024
    A company that focuses on development of innovative prescription products for aesthetic medicine and medical dermatology is looking for CMO to manufacture Liniment for the treatment of Crow’s feet and hyperhidrosis. The required packaging is 1 ml in dropper. The project launch time is in 2026. The required quantity is 10 batches of 100 kg. The country of distribution is United States. The geographical preference for service provider is United States.
    22 Feb 2024
  • A company based in United States that focuses providing solutions in areas specifically defense, intelligence, health & bioscience, transport, energy and critical infrastructure is looking for GMP certified CDMO for intravenous injectables. The country of distribution is United States.
    09 Feb 2024
    A CMO that focuses on manufacturing, licensing & marketing of various OTC & Rx finished formulations is looking for a GMP certified CDMO for Tech Transfer of Solid, Liquid and Semi-Solid finished formulations. The projected annual manufacturing volume is 30 MT – 1000 MT. The country of distribution is Europe & United Kingdom and the geographical preference for service provider is Europe.
    20 Jan 2024
  • A company that focuses on manufacturing and distribution of various finished formulations including tablets, capsules, dry powder sachets and ointments is looking for suppliers of Various Excipients for commercial purposes. The suppliers must support this enquiry with DMF & CoA.
    1. USP /BP Grade Butylated Hydroxy Toluene (1 kg) Excipient
    2. Hydroxy Propyl Methyl Cellulose Excipient
    03 May 2024
    A CDMO that focuses on manufacturing, development & distribution of various non-sterile oral dosage forms is looking for suppliers of Ph. Eur. Grade Dichloromethane (6 Tons) Excipient for commercial purposes. The supplier must support this enquiry with CEP & DMF.
    23 Apr 2024
  • A U.S.- domiciled publicly traded generics and specialty pharmaceutical company is looking for suppliers of USP Grade Sodium Deoxycholate Excipient for development purposes. The supplier must support this enquiry with GMP & CoA.
    22 Apr 2024
    A company that deals in the import, export and distribution of various pharmaceutical products is looking for suppliers of Pharma Grade Coco Diethanolamide (25 kg) Excipient for commercial purposes. The supplier must support this enquiry with CoA.
    20 Apr 2024

Interviews #SpeakPharma

  • “Through innovation, we’ve emerged as world leaders in biopolymers”
    This week, SpeakPharma interviews Anne-Laure Gaudry, Head of Innovation and R&D at HTL Biotechnology, a global producer and developer of pharmaceutical-grade biopolymers. Anne-Laure Gaudry discusses the story of HTL Biotechnology, the evolution of the biopolymer market, and HTL’s innovation and R&D strategy. Excerpts: 🔑 HIGHLIGHTS// pharmaceutical-grade biopolymers/ CDMO Can you briefly take us through the history of HTL Biotechnology? From the very beginning, HTL Biotechnology distinguished itself from the rest through its bacterial fermentation manufacturing method, as also its hyaluronic acid produced in fiber form. These are proof of our uniqueness, very high product quality, experience and the unique know-how of our teams. For over 30 years, HTL Biotechnology has been producing hyaluronic acid (HA) for some of the biggest names in the pharmaceutical industry. World-renowned expertise and unwavering commitment of HTL Biotechnology’s teams has helped the company grow significantly over the years. Since 2003, HTL Biotechnology has embarked on a process of improving its manufacturing facilities and final purification stages. This has significantly increased the purity of the pharmaceutical grade HA that we produce. To consolidate the laboratory’s lead in the market in terms of product quality, HTL Biotechnology invested heavily in training, quality control and better equipment. In 2014, to keep pace with demand and to ensure HTL Biotechnology’s long-term growth, the Javené site (Brittany, France) was considerably expanded. At the same time, HTL Biotechnology continued to strengthen its teams, infrastructure, and equipment, notably through the acquisition of new fermenters with greater capacities. Over the years, HTL Biotechnology has become the world leader in pharmaceutical grade biopolymers and a unique force in innovation. To bring innovation for its customers in historical applications (aesthetics, rheumatology, ophthalmology) and to pave the way in new therapeutic applications (drug delivery, regenerative medicine, microneedling, ocular drug delivery and bioprinting), HTL Biotechnology decided to invest in the construction of an R&D laboratory, called HTL3, in Javené, France.  Inaugurated in 2018, this state-of-the-art laboratory symbolizes the company’s R&D ambitions, to push the boundaries of the use of HA to meet unmet medical needs. 🔑 HIGHLIGHTS// manufacturing HA for 30 years/ hyaluronic acid in fiber form/ Javené site expansion/ regenerative medicine, microneedling, ocular drug delivery and bioprinting How has the market for biopolymers evolved over the years? As the world became more aware of the environment and began moving towards sustainability, the demand for biopolymers increased. In the pharma sector, biopolymers began to see substantial use in drug delivery methods to finetune efficacy. Biopolymers are an important class of materials because of their biodegradability — they work well with the body, are safe, don’t trigger immune responses, stay in the bloodstream for a long time, and can carry a high amount of both large and small drug molecules. The quality of hyaluronic acid has always been a priority for HTL. The first few years of our activity in biotechnology — i.e. between 1992 and 1998 — were a period of finetuning the methods for producing HA by bacterial fermentation, in order to find the parameters that would ensure the best possible quality for use by the pharmaceutical industry. Since then, HTL Biotechnology’s quality teams have set up a quality management system. Today, we are ISO 14001 certified. Over the past few decades, various methods and procedures for producing biomaterials have emerged that aim to understand and replicate the crucial structural and compositional features of natural tissues. We’ve been using bacterial fermentation to produce HA since the early 1990s and are one of the most experienced companies in this space. Today, raw materials of animal origin are no longer needed to produce HA, thereby preserving natural resources. Over the last few decades, our HA has changed the lives of millions of people around the world. 🔑 HIGHLIGHTS// DDS/ biodegradability/ don’t trigger immune response In 2021, the company opened a new bioproduction unit in France. Tell us how the market for HA is growing, and how the new unit has contributed to growth. We have unparalleled expertise in producing premium quality HA. We had been experiencing double-digit growth and international expansion prior to setting up of the new bioproduction unit in France. Therefore, we strategically made the largest investment ever for a biopolymer production unit. The over €50 million (US$ 53.52 million) investment in HTL4 signifies the culmination of HTL Biotechnology’s biomanufacturing expertise, setting a new standard for innovation and infrastructure quality. Cutting-edge technologies at the plant enable production lines to be automated and digitized, guaranteeing historic quality of production. From the outset, we took a strategic decision to reduce the environmental impact of our activities while guaranteeing reliability. This unit has more than doubled our production capacity, allowed us to accelerate international development and emerge as the world’s largest producer of pharmaceutical-grade HA.  Finally, HTL4 has secured the supply of our customers in over 30 countries and helped many leading pharma companies offer innovative therapeutic solutions to their patients worldwide. 🔑 HIGHLIGHTS// double-digit growth/customers in over 30 countries/ €50 million investment HTL Biotechnology also has a 45-year track record in producing DNAs. Which applications require DNAs? And what goes behind DNA production? We are identified with our quality, safety and efficacy. The market has recognized us for being able to provide pharmaceutical-grade DNA for both topical and injectable applications, with a high level of purity, biocompatibility and efficacy, owing to our gentle production process designed to protect the double-strand structure of a DNA. All our products are GMP compliant. Polynucleotides have pharmaceutical uses in aesthetics. They help increase collagen production in the skin and maintain its elasticity. Polynucleotides also promote fibroblasts proliferation that are essential for wound healing. PDRN is a drug used to reduce inflammation caused by UVA and UVB, and it also reduces oxidative stress in cells. We also produce sodium DNA, our cosmetic grade DNA used in products like regenerating mask, serum, cream and repairing cream. 🔑 HIGHLIGHTS// topical and injectable applications/ high level of purity/ help increase collagen production in skin and maintain its elasticity What are some of the objectives of your R&D strategy? Innovation is at the heart of our strategy. Our specialist teams work seamlessly to drive innovation. We believe biopolymers are central to tomorrow’s therapeutic innovations and have the potential for infinite applications in many therapeutic areas. Our strategy is to innovate for the benefit of our customers and their patients through the development of increasingly avant-garde and high-performance biopolymer platforms. Today, HTL Biotechnology produces over a hundred ‘custom-made’ HAs for its customers. We have developed several new products, such as silanized HA and methacrylate HA. With chemical functionalization, new properties and characteristics can be added to the polymer. HTL Biotechnology’s functionalized biopolymers business enables the development of tailor-made products that can be manufactured on an exclusive basis, from process development to GMP production. These processes can be used to create the HAs of tomorrow. 🔑 HIGHLIGHTS// development of increasingly avant-garde and high-performance biopolymer platforms What are some of the new growth areas HTL Biotechnology is looking at ? There are some very exciting possibilities for HA in a few rapidly developing technologies like bioprinting and microneedle patches. Today, one million people in the world are awaiting transplants. Can you imagine the possibility of creating organs? Bioprinting is the biological equivalent of 3D printing. HA is one of the substances used for bioprinting. The technology allows us to imagine a fantastic area for expansion. Moreover, we are looking at intradermal vaccine delivery, thanks to dissolvable needles that are barely visible to the naked eye and are made of HA. We are also working on innovation in other areas such as oncology, rheumatology and odontology. 🔑 HIGHLIGHTS// possibility of creating organs?/ 3D printing/ intradermal vaccine delivery/ Over the last few years, HTL Biotechnology has set up an affiliate in Asia. How have these affiliates contributed to the growth of HTL Biotechnology? In 2022, we established an Asian subsidiary, and this can be seen as a mark of the company’s ongoing global expansion and dedication to serving healthcare customers across all Asian countries. Operating from Singapore, HTL Biotechnology Asia will bring the company closer to its clients and ensure unparalleled support. Also, our teams in Korea and China are focused on engaging with our existing clients, forging new business relationships, and exploring opportunities for expanding our market presence in these regions. 🔑 HIGHLIGHTS// Asian subsidiary, in Singapore What are the company’s long-term growth plans? Are you looking at expanding your global presence? Our story has only just begun. By 2030, we expect our innovative biopolymer platform to benefit over 500 million patients worldwide suffering from ocular, rheumatological, aging diseases and other diseases with the development of new applications. Our future involves a global expansion, from the United States to Asia, with stronger teams in France, an ever-increasing number of applications for our biopolymers, and the constant creation of new and innovative biopolymers, thanks to our R&D investments. We look at HTL Biotechnology as a global company with a heart in Brittany, France. 🔑 HIGHLIGHTS// 500 million patients/ ocular, rheumatological and aging diseases/ global expansion to the US and Asia/

    Impressions: 326

    https://www.pharmacompass.com/speak-pharma/through-innovation-we-ve-emerged-as-world-leaders-in-biopolymers

    01 May 2024

Data Compilation & Company Tracker #PharmaFlow

  • Top Pharma Companies & Drugs in 2023: Merck’s Keytruda emerges as top-selling drug; Novo, Lilly sales skyrocket
    The pharma industry clearly recalibrated itself in 2023, turning its focus away from Covid and onto two of the biggest threats to human health – obesity and cancer. The top lines of the major pharma companies reflect this shift in focus.We always knew that Pfizer’s record US$ 100 billion revenue for 2022 wasn’t sustainable. Even though Pfizer’s 2023 sales were lower by nearly 42 percent against its 2022 sales, the New York-headquartered drugmaker managed to retain its pole position. The two main reasons behind its ‘top of the charts’ sales of US$ 58.5 billion were Pfizer’s record nine new molecular entity approvals by the US Food and Drug Administration (FDA) and the launch of its vaccine for respiratory syncytial virus (RSV).Johnson & Johnson came second with sales of US$ 54.8 billion (excluding its consumer business and MedTech units). AbbVie took bronze despite Humira being subject to biosimilar competition and Merck maintained its fourth position. Roche nabbed the fifth position from Novartis (which stood sixth). Bristol Myers Squibb maintained its position at seven, as did AstraZeneca (eighth) and Sanofi (ninth). And Eli Lilly bumped into the tenth spot, knocking out GSK.View Our Interactive Dashboard on Top Drugs in 2023 by Sales (Free Excel Available)Keytruda, Eliquis, Humira top charts; Novo’s Ozempic debuts top 10 list at number fourMerck’s Keytruda became the number one selling drug in the world, a position that was held by AbbVie’s Humira for long, and Pfizer’s Comirnaty in the Covid years. This oncology drug raked in a whopping US$ 25 billion, with sales increasing 19 percent last year. In fact, Keytruda accounted for 46.7 percent of Merck’s pharmaceutical sales, which grew 3 percent in 2023 to US$ 53.6 billion.At number two was Pfizer and BMS’ anticoagulant Eliquis — it posted global sales of US$ 18.95 billion (marking a growth of 4 percent on 2022 sales). With competition from generics, Humira’s sales fell by 32 percent to US$ 14.5 billion. As a result, this blockbuster anti-rheumatic drug fell to the third rank.The fourth spot was taken up by Novo Nordisk’s Ozempic, the wonder drug that treats type 2 diabetes. Gilead’s Biktarvy, a med that treats HIV-1, saw sales jump 14 percent — from US$ 10.39 billion posted in 2022 to US$ 11.85 billion last year. This way, Biktarvy emerged as the fifth largest selling drug of 2023.At number six was Sanofi and Regeneron’s Dupixent. This allergic diseases med posted 11-figure sales in 2023, netting € 10.72 billion (US$ 11.59 billion) globally, a growth of 34 percent over 2022 numbers.At number seven was J&J’s biggest blockbuster immunology drug Stelara that raked in US$ 11.3 billion in 2023. Coming a close eighth was Pfizer-BioNTech’s Covid-19 vaccine Comirnaty — its sales fell by over 70 percent to US$ 11.22 billion in 2023. At the ninth spot was Lilly and Boehringer’s diabetes drug Jardiance that saw a 27.7 percent increase in total global sales at US$ 10.6 billion. And rounding off the list at number 10 is BMS’s Opdivo, a Keytruda rival. Opdivo hauled in US$ 10 billion in total global sales in 2023, a year-on-year increase of 8 percent.View Our Interactive Dashboard on Top Drugs in 2023 by Sales (Free Excel Available)Driven by diabetes, obesity care meds, Novo, Lilly post double-digit sales growthDemand for diabetes and new weight-loss drugs catapulted Novo Nordisk to emerge as the most valuable public company in Europe. Its net sales zoomed 31 percent to DKK 232.3 billion (US$ 33.75 billion) compared to DKK 177 billion (US$ 25.8 billion) in 2022. Net profit jumped 51 percent to DKK 83.68 billion (US$ 12.51 billion) in 2023 from DKK 55.5 billion (US$ 8.32 billion) in 2022 — the highest annual profit for the Danish drugmaker in over three decades.The growth was driven by Ozempic, whose sales spiked 60 percent in 2023 to DKK 95.7 billion (US$ 13.91 billion), from DKK 59.8 billion (US$ 8.71 billion) the year before.Rival Eli Lilly’s revenue grew 20 percent in 2023 to US$ 34.1 billion from US$ 28.5 billion in 2022. Mounjaro turned out to be a star for the Indianapolis drugmaker with its sales rocketing 970 percent in 2023 to US$ 5.16 billion. FDA also approved it to treat obesity under the brand name Zepbound in November, which brought in additional revenues of US$ 176 million.View Our Interactive Dashboard on Top Drugs in 2023 by Sales (Free Excel Available) GSK’s RSV jab makes strong debut; AbbVie’s immunology drugs post steep growthGSK’s Arexvy was the first RSV vaccine approved by the FDA. It made a strong debut — Arexvy contributed £ 1.2 billion (US$ 1.5 billion) to GSK’s sales in just four months.AbbVie posted another solid financial year. Though the drop in Humira revenue was offset by two newer immunology blockbuster drugs, Skyrizi and Rinvoq, the Illinois-headquartered drugmaker did posted a marginal decrease in revenue of 6.4 percent to US$ 54.3 billion. However, revenue from Skyrizi soared 50 percent to US$ 7.8 billion, while Rinvoq’s sales increased 57 percent to US$ 4 billion. AbbVie expects a combined US$ 16 billion from Skyrizi (US$ 10.5 billion) and Rinvoq (US$ 5.5 billion) sales in 2024. BMS attributed its 2 percent decrease in revenue (of US$ 45 billion) to lower sales of Revlimid in the US due to competition from generics. Sales of the multiple myeloma treatment dropped 39 percent to US$ 6.1 billion. Ophthalmology drug Eylea saw a drop in sales  of 4 percent, at US$ 9.21 billion (from US$ 9.65 billion), as competition from Roche’s Vabysmo triggered a price cut by Regeneron. Vabysmo saw sales balloon 324 percent from CHF 591 million (US$ 685.56 million) to CHF 2.4 billion (US$ 2.78 billion) in 2023.View Our Interactive Dashboard on Top Drugs in 2023 by Sales (Free Excel Available) Our viewAccording to data analytics company GlobalData, GLP-1 agonist drugs (such as Ozempic and Mounjaro that treat type 2 diabetes) are slated to overtake PD-1 antagonists (such as oncology drugs Keytruda and Opdivo) as the top-selling drugs on the market in 2024. It estimates a robust compounded annual growth rate (CAGR) of 19.2 percent from 2023 to 2029 for GLP-1 drugs that seem to have more benefits besides bringing down blood sugar levels (such as weight management, benefits to the heart etc).The market size for GLP-1 is likely to increase to US$ 105 billion by 2029. In contrast, the data firm projects a CAGR of 4.7 percent in the PD-1 antagonist market, with its market size projected to be around US$ 51 billion in 2029. Given these projections, we are likely to see more movers and shakers in our top 10 drug list this year.

    Impressions: 1287

    https://www.pharmacompass.com/radio-compass-blog/top-pharma-companies-drugs-in-2023-merck-s-keytruda-emerges-as-top-selling-drug-novo-lilly-sales-skyrocket-due-to-glp-1-drugs

    #PharmaFlow by PharmaCompass
    25 Apr 2024

Monthly Stock Recap #PipelineProspector

  • Pipeline Prospector April 2024: Indices dip amid muted Q1 results; Vertex acquires Alpine Immune for US$ 4.9 bn
    Pharma indices had begun to recede in March. Their red streak accelerated in April with the Nasdaq Biotechnology Index (NBI) falling 6 percent from 4429.97 in March to 4162.33 last month and the SPDR S&P Biotech ETF (XBI) index tripping 10 percent from 94.34 to 84.62. Similarly, the S&P Biotechnology Select Industry Index (SPSIBI) was down 11 percent from 7402.50 to 6584.40 in April.This muted performance was also reflected in the first quarter (Q1) results. Biogen, Biomarin, Roche, Gilead, Merck, Sanofi, BMS and Johnson & Johnson announced their Q1 results in April. While Roche and Biogen reported a drop in revenues, BMS posted a loss in Q1, even though its revenues increased. And Sanofi reported a 14.7 percent drop in operating income due to competition from generics and currency fluctuations. BioMarin, Gilead and Merck reported a 9 percent, 5 percent and 9 percent increase, respectively, in their Q1 revenues over Q1 2023.There were a handful of deals announced last month, the biggest being Vertex Pharmaceuticals’ acquisition of Alpine Immune Sciences for US$ 4.9 billion. The deal gives Vertex access to Alpine’s protein-based immunotherapies for autoimmune diseases.Japanese drugmaker Ono Pharmaceutical agreed to acquire Massachusetts-based Deciphera Pharmaceuticals for US$ 2.4 billion. The acquisition gives Ono access to Deciphera`s oncology pipeline. Denmark’s Genmab agreed to acquire privately-owned ProfoundBio for US$ 1.8 billion. ProfoundBio has three next-generation antibody drug conjugate (ADC) candidates in its pipeline that will now go to Genmab.Access the Pipeline Prospector Dashboard for April 2024 Newsmakers (Free Excel)FDA okays ImmunityBio’s Anktiva, Day One’s Ojemda for bladder, brain cancerLike March, April too saw several significant drug approvals, especially in oncology. ImmunityBio (its stock was up 50 percent in April) won its first US Food and Drug Administration (FDA) approval as the agency greenlit Anktiva as part of a combination therapy to treat a type of bladder cancer. With this approval, Anktiva will compete with Merck’s Keytruda.AstraZeneca (stock up 12 percent) and Daiichi Sankyo’s Enhertu has been granted accelerated approval in the US to treat adult patients with HER2-positive solid tumors that have spread or cannot be surgically removed. These patients have undergone prior treatment and have no satisfactory alternatives available to them. J&J and Legend’s Carvykti has become the first and only BCMA-targeted therapy approved by the FDA for patients with relapsed or refractory multiple myeloma, who have received just one prior line of treatment. The approval is an important milestone in J&J’s plans to make Carvykti a US$ 5 billion-plus asset at peak yearly sales.Day One Biopharmaceuticals’ Ojemda has been granted FDA’s accelerated approval to treat certain types of pediatric brain cancer. The pan-RAF kinase inhibitor has been okayed for patients six months of age and older with relapsed or refractory pediatric low-grade glioma (LGG) harboring a BRAF fusion or rearrangement, or BRAF V600 mutation. This is the first FDA approval of a systemic therapy for treating what is the most common form of childhood brain tumor.Access the Pipeline Prospector Dashboard for April 2024 Newsmakers (Free Excel) Basilea’s antibiotic bags FDA nod; Vanda’s Fanapt approved for bipolar disorderThe agency also approved Vanda Pharmaceuticals’ (stock up 25 percent) Fanapt tablets for treating manic or mixed episodes associated with bipolar-1 disorder in adults. The atypical antipsychotic agent has been used for the treatment of patients with schizophrenia since its FDA approval in 2009. This second approval for bipolar-1 disorder patients (who experience manic episodes that last at least seven days) could help revive Fanapt prescriptions.FDA has also approved Basilea Pharmaceutica’s Zevtera, an antibiotic for bacterial infections including multidrug-resistant strains. The US agency has okayed it for three conditions – treatment of adults with Staphylococcus aureus bacteremia, including those with right-sided infective endocarditis; adults with acute bacterial skin and skin structure infections; and adult and pediatric patients with community-acquired bacterial pneumonia.Access the Pipeline Prospector Dashboard for April 2024 Newsmakers (Free Excel) BMS’ schizo drug shows benefit sans weight gain; Imfinzi scores in lung cancer trialA common side effect associated with anti-psychotics is weight gain. However, interim results from a late-stage trial have shown that BMS’ schizophrenia drug KarXT continued to improve symptoms of the severe mental disease even at 52 weeks, and without weight gain.In another phase 3 trial, Imfinzi significantly improved overall survival and progression-free survival in patients with limited-stage small cell lung cancer. This makes this blockbuster drug the first and only immunotherapy to demonstrate survival benefit for this aggressive form of lung cancer. Imfinzi had posted sales of US$ 4.24 billion in 2023.Intra-Cellular Therapies said a phase 3 study of its drug Caplyta in people with major depressive disorder (MDD) met both its primary and key secondary endpoints. Given once daily as an adjunctive therapy to antidepressants, Caplyta 42 mg significantly beat the placebo at improving depression severity.Access the Pipeline Prospector Dashboard for April 2024 Newsmakers (Free Excel) Zepbound shows benefit in sleep disorder; Novartis’ Fabhalta reduces proteinuriaEli Lilly’s popular weight-loss drug Zepbound cut irregular breathing episodes associated with a common sleep-related disorder – obstructive sleep apnea (OSA). Treatment with Zepbound reduced the frequency of irregular breathing episodes by as much as 63 percent in adults with OSA and obesity across two late-stage trials. Lilly plans to submit the findings to FDA to expand Zepbound’s use for OSA. Roche’s Genentech said its drug Columvi, in combination with chemotherapy, demonstrated a statistically significant improvement in overall survival for people with relapsed or refractory diffuse large B-cell lymphoma (DLBCL). A late-stage study pitted the Columvi-chemotherapy combination against a rituximab-chemotherapy combination in patients who received at least one prior line of therapy and are not candidates for autologous stem cell transplant. Patients in the Columvi group lived longer.In another late-stage trial, Novartis` drug Fabhalta reduced proteinuria (protein in the urine) in patients with IgA nephropathy by 38.3 percent. The Swiss drugmaker filed for FDA’s accelerated approval using the data, and the agency has granted it priority review.Access the Pipeline Prospector Dashboard for April 2024 Newsmakers (Free Excel) Our viewAt the start of 2024, the US market saw inflation falling and there were talks of interest rate cuts by the Federal Reserve. But few months on, the outlook has darkened a bit with inflation refusing to let off steam and economic output slowing down in the US. This is getting reflected in the pharma indices and the Q1 results of several drugmakers. Though overall, we have faith in the pharma sector’s spirit of innovation and its zest for dealmaking. Despite the macroeconomic challenges, there is hope that the other three quarters of 2024 will look better.Access the Pipeline Prospector Dashboard for April 2024 Newsmakers (Free Excel) 

    Impressions: 244

    https://www.pharmacompass.com/pipeline-prospector-blog/pipeline-prospector-april-2024-indices-dip-amid-muted-q1-results-vertex-acquires-alpine-immune-for-us-4-9-bn

    #PipelineProspector by PharmaCompass
    09 May 2024

Weekly News Recap #Phispers

  • FDA to consider psychedelic-assisted drug for treating PTSD; Novartis buys Mariana Oncology for up to US$ 1.75 bn
    Last year, the US Food and Drug Administration (FDA) had published a new draft guidance for researchers investigating the use of psychedelic drugs for potential treatment of psychiatric disorders. This week, the agency took a major step in that direction by announcing that its panel of independent advisers will deliberate on June 4 on whether it should recommend approving the first midomafetamine-assisted therapy for post-traumatic stress disorder (PTSD). Midomafetamine or MDMA is a psychedelic, commonly known as ecstasy.In deals, Novartis has acquired Massachusetts-based radioligand therapy developer Mariana Oncology for an upfront payment of US$ 1 billion plus US$ 750 million in additional milestone payments.After much delay, FDA has announced that its panel of independent advisers will discuss Eli Lilly’s experimental Alzheimer’s disease drug donanemab on June 10.In trials, Regeneron’s investigational gene therapy (DB-OTO) dramatically improved hearing to normal levels in a child with profound genetic deafness within 24 weeks. Pfizer’s mid-stage trial of its experimental gene therapy to treat Duchenne muscular dystrophy (DMD) took a tragic twist when a young patient died. And AstraZeneca clinched a late-stage win for Calquence in untreated mantle cell lymphoma. Meanwhile, Pfizer has agreed to settle over 10,000 lawsuits pertaining to cancer risks concerning the now discontinued heartburn drug Zantac.After over three billion doses, the Oxford-AstraZeneca Covid vaccine is being withdrawn worldwide. And in compliance news, Indian drugmaker Zydus Lifesciences got issued a second Form 483 in one month.Novartis dishes out US$ 1.75 bn for Mariana to strengthen radioligand med pipelineNovartis has agreed to buy Massachusetts-based Mariana Oncology for an upfront payment of US$ 1 billion plus US$ 750 million in additional milestone payments. Preclinical-stage biotech Mariana focuses on developing novel radioligand therapies (RLTs) to treat cancers with high unmet need. The acquisition encompasses a robust portfolio of RLT programs spanning lead optimization to early development across a range of solid tumor indications such as breast, prostate and lung cancer. RLTs are a form of precision medicine that combines a tumor-targeting molecule (ligand) with a therapeutic radioisotope (a radioactive particle). This targeted approach enables the delivery of radiation to the tumor, while limiting damage to the surrounding cells.In a first, FDA panel to consider psychedelic-assisted therapy for PTSDFDA’s panel of independent advisers will deliberate on June 4 to discuss whether it should recommend approving the first MDMA-assisted therapy for PTSD, said Lykos Therapeutics, a drugmaker working in the mental healthcare space. MDMA (or midomafetamine) is a psychedelic, commonly known as ecstasy. This will be the first FDA advisory committee meeting to review a potential new PTSD treatment in 25 years.PTSD is a mental health condition triggered by a terrifying event. For long, mental health researchers have been captivated by psychoactive ingredients found in cannabis and LSD. A number of companies are testing such drugs to find cures for a range of mental health disorders.Meanwhile, a London-based biotech — Compass Pathways — has announced top-line results from a phase 2 study evaluating the safety and tolerability of an investigational psilocybin treatment (COMP360) in 22 patients with PTSD. The study met its primary safety endpoint and available secondary efficacy endpoints. Psilocybin is a naturally occurring psychedelic compound.Panel to meet on June 10 to discuss Lilly’s donanemab: On June 10, FDA’s panel of independent advisers will discuss Eli Lilly’s experimental Alzheimer's drug donanemab. The drug was declined accelerated approval in January 2023. If approved, it will compete with Eisai and Biogen’s Leqembi (lecanemab-irmb), which saw FDA approval last year.AstraZeneca to withdraw Covid vaccines globally, cites surplus of newer vaccinesAstraZeneca has said it has begun a worldwide withdrawal of its Covid vaccine — Vaxzevria, also sold as Covishield — due to the surplus availability of other updated vaccines. Astra denied the decision had anything to do with the claim that the vaccine caused unusual blood clots, which were sometimes fatal. This easy to store vaccine was once heralded as “a vaccine for the world.” “As multiple, variant Covid-19 vaccines have since been developed there is a surplus of available updated vaccines,” the company said.Pfizer reports patient death in phase 2 study on DMD: A young patient died from cardiac arrest after receiving Pfizer’s experimental gene therapy as part of a mid-stage trial for the muscle-wasting disorder Duchenne muscular dystrophy (DMD), the company said. The patient received the investigational gene therapy, fordadistrogene movaparvovec, in early 2023. Pfizer is in the process of reviewing the data to understand the potential cause.Meanwhile, the drug behemoth has agreed to settle over 10,000 lawsuits pertaining to cancer risks concerning the now discontinued heartburn drug Zantac, a Bloomberg News report said.Astra clinches late-stage win for Calquence in untreated mantle cell lymphomaIn a phase 3 study, AstraZeneca’s Calquence (acalabrutinib) in combination with standard-of-care chemoimmunotherapy, bendamustine and rituximab, demonstrated a statistically significant and clinically meaningful improvement in progression-free survival (PFS) as compared to standard of care in previously untreated adult patients with mantle cell lymphoma (MCL). While this came from interim analysis, it renders Calquence the first BTK inhibitor to show a favorable trend in overall survival versus standard-of-care chemoimmunotherapy in previously untreated MCL.Regeneron’s gene therapy ‘dramatically’ improves hearing in kidsRegeneron Pharmaceuticals’ investigational gene therapy DB-OTO dramatically improved hearing to normal levels in a child with profound genetic deafness within 24 weeks in phase 1/2 trial. The child, the youngest in the world to receive a gene therapy for genetic deafness, was dosed at 11 months of age. In a second child, dosed at four years of age, initial hearing improvements were observed at six weeks.Zydus’ Gujarat plant hit with Form 483 with 10 observationsZydus Lifesciences has received its second Form 483 within a span of one month. Following an inspection at the company’s site in the Indian state of Gujarat between April 15 and April 23, FDA issued a Form 483 with 10 observations. The agency found that Zydus skirted and skipped over procedures that prevent microbiological contamination of sterile drug products. After cross-contamination was found and batches rejected, other lots made with the same equipment were shipped to the US without thoroughly being investigated. Furthermore, an employee was reported to be collecting samples but had not actually done so. The task was instead delegated to an unqualified staffer.  

    Impressions: 327

    https://www.pharmacompass.com/radio-compass-phisper/fda-to-consider-psychedelic-assisted-drug-for-treating-ptsd-novartis-buys-mariana-oncology-for-up-to-us-1-75-bn

    #Phispers by PharmaCompass
    09 May 2024

Content #LearnMore

  • View Sharp
    View Sharp's clinical trial supply & contract pharmaceutical packaging services for injectables and oral dosage forms on PharmaCompass. What is pharmaceutical contract packaging and how is Sharp a reliable packaging partner for the pharmaceutical and biotech industries? Pharmaceutical packaging can be defined as a set of operations including filling, sealing, packaging, and labeling of semi-finished or finished products. Pharma packaging is an economical means to present, preserve, identify, provide information, maintain product integrity, and ensure stability. It also plays a crucial role in the transportation of sensitive and strictly controlled products. Pharmaceutical contract packaging refers to packaging that is executed and supplied by a licensed third-party service provider that comprises both initial packaging and repackaging. These contract packaging service providers may offer clinical and commercial packaging solutions for pharmaceutical products. Pharmaceutical contract packaging organizations are well-equipped to offer a comprehensive range of primary, secondary, and tertiary packaging solutions. Primary packaging surrounds the pharmaceutical formulation and includes bottles, blisterings, pouches, sachets, tubes, auto-injector pens, etc. Whereas secondary packaging offers further external protection and includes artwork design, labeling for parenteral and injectables, child-resistant and compliance prompting packaging, etc. Additionally, tertiary packaging is used during transportation to absorb physical impacts, moisture, and dust and includes cardboard boxes, stretch wraps, shrink films, and wooden and plastic pallets. Sharp is a leading contract packaging organizations that offer pharmaceutical packaging services among others. It has more than 70 years of experience in pharmaceutical clinical packaging, clinical trial supply services, and small-scale sterile manufacturing. Sharp has more than 2,000 employees who work in its state-of-the-art GMP facilities in the US, UK, Belgium, and the Netherlands. Sharp, offers contract manufacturing and packaging services and support from phase I clinical trial supplies to commercial launch and lifecycle management to its pharmaceutical and biotechnology partners across the world. It has deep expertise in clinical trial packaging and labeling along with a skilled global design team that utilizes cutting-edge software and technology ensuring patient-friendly and differentiated packaging for drug products. Apart from this, Sharp is also a reliable partner for sourcing packaging material and offers integrated pharmaceutical packaging and labeling services along with over-encapsulation of oral solids and the production of placebo capsules for study blinding. Sharp is a contract packaging organization that offers commercial packaging services including contract blister packaging services, bottle packaging, sachet packaging, injectable packaging, and other solid dose packaging solutions. Additionally, it offers clinical packaging and labeling solutions such as clinical trial material packaging, clinical trial packaging and labeling, clinical trial logistics and packaging, and clinical trial supply services, or clinical supplies. Its clinical and commercial packaging services are outlined below: Clinical Packaging Solutions Sharps clinical packaging solutions encompass primary packaging and labeling and secondary packaging. Its pharmaceutical primary packaging offers reliable clinical packaging services, clinical supply chain services, primary packaging solutions, and cold-chain secondary packaging and labeling at 2-8°C, -20°C, and even at -70°C. Sharp also provides reliable clinical pharma packaging services and labeling, secondary packaging solutions, pharmaceutical clinical packaging and labeling solutions along with expertise and capabilities in handling cold-chain pharmaceutical labeling and packaging from 2-8°C to -70°C. Commercial Packaging Solutions For more than 65 years, Sharp has been providing a full range of commercial primary and secondary packaging solutions, blister packaging, and contract manufacturing and packaging services for pharmaceutical oral solid dosage forms. It offers contract blister packaging services and bottle packaging for pharmaceutical drug products. Apart from this Sharp provides pharma packaging contract services for small and large-volume batch sizes of injectables. It offers pharmaceutical packaging services for cold chain storage, packaging in temperature- and light-controlled environments, serialization, and customized distribution. Additionally, Sharp is involved in the pharma packaging of oral solids, liquids, and semi-solids. Moreover, Sharp is a premier commercial packaging service provider for high-value, low-volume gene therapy. It also offers pharmaceutical packaging services, expertise, and powerful technology that facilitates product serialization and aggregation. Therefore, Sharp’s pharma packaging contract services, spanning from clinical supplies to commercial include pharma clinical trial material manufacturing, clinical primary packaging services, clinical secondary packaging solutions, clinical trial packaging and labeling, and clinical trial logistics and packaging. Furthermore, Sharp’s contract manufacturing and packaging services encompass commercial pharma packaging solutions and labeling and supply services. Consequently, all the aforementioned offerings position Sharp as a one-stop-shop contract pharmaceutical packaging service provider for clinical and commercial scales. How does Sharp address challenges related to clinical labeling and secondary packaging? Sharp has over 70 years of experience and is a pioneer in clinical trial supply services and pharmaceutical packaging. Dedicated to the right-first-time principle, Sharp is a reliable partner for secondary packaging and clinical pharmaceutical labeling and packaging. It offers a wide range of quick, scalable clinical trial packaging services and labeling and packaging solutions in all formats, with capabilities spanning the complete lifespan of investigational medicinal products (IMPs). Moreover, Sharp can also address challenges related to packaging and labeling and offers pharmaceutical packaging and labeling services and clinical packaging and labeling services to its clients. Additionally, its clinical packaging and labeling solutions also include in-house auxiliary variable data printing outsourced booklet labels, client-supplied randomization fully supported, and annex 13 compliant and 21 CFR Part 11 compliant PRISYM software for label design. Sharp's pharmaceutical packaging and labeling services include single and multi-panel labels and booklets, 2D barcoding capabilities, randomized and open, 128 barcoding. It also offers regulatory and translation services, sequentially numbered, variable text, code break, and randomized generation among other clinical packaging and labeling solutions. Sharp is a leader in providing pharmaceutical clinical packaging, contract packaging services, and labeling and supply services in compliance with strict regulatory guidelines. It has special pharma packaging and labeling expertise and capabilities for packaging drug products. Sharp addresses various challenges related to pharma packaging and labeling which includes: Sharp can provide cold-chain pharmaceutical labeling and packaging from 2-8°C to -70°C for drug products that need low temperatures for their transportation and storage. Sharp can support the secondary packaging for most complex drug candidates, such as controlled substance packaging (DEA schedule I-V), and has the capabilities to scale up to commercial supplies. Its design and logistics staff can also assist with the challenges of blinding products and syringes for clinical trial services. Sharp does this by providing annex 13 compliant and 21 CFR Part 11 compliant PRISYM software for label design, client-supplied randomization fully supported, and in-house auxiliary variable data printing outsourced booklet labels. With issues related to timely delivery and efficient labeling, Sharp provides pharmaceutical labeling and packaging solutions by using Scan assembly technology and Interactive Response Technologies (IRT), storage, and distribution. To overcome the label readability issues for clients worldwide, Sharp designs and prints multilingual clinical labels. Therefore, Sharp acts as a one-stop-shop packaging organization that provides pharmaceutical contract packaging services, clinical primary packaging services, primary and secondary clinical packaging, and labeling and supply services to its clients worldwide. What range of packaging design and kitting services does Sharp offer? Sharp is a market leader in the design and delivery of primary and secondary packaging. Due to its structural, graphic, and design engineers as well as its understanding of supply chain and regulatory issues, Sharp excels in pharmaceutical packaging. Sharp has years of experience in creating cutting-edge pharma packaging solutions. It is skilled in brand creation, modifying current artwork, marketing research, FDA filing standards, 3D rendering, senior, child-friendly, or child-resistant design, and labeling and supply services. Sharp's global design team provides the creativity and accuracy required to design highly functional and compliant primary and secondary commercial and clinical pharma packaging services. Sharp offers a wide range of design services and pharmaceutical packaging solutions using the latest tools and technologies to guarantee premium and user-friendly product packaging. Additionally, it provides structural and graphic design development for quick launch and regular upgrades for commercial artwork. Sharp’s wide range of packaging design services for pharmaceutical products includes: Artwork Design Services: Sharp can provide pharma packaging contract services including customized artwork as per specific markets from initial mock-ups to product registration. Packaging Samples: Sharp’s contract pharmaceutical packaging services can create production-quality models for use in marketing presentations, human factor research, and photography that closely match the commercial package. Tray Design: Sharp precisely assesses product components to create a tray design that best suits the drug. 3D Printing: Sharp can rapidly confirm that all product components fit by using its technology to create 3D printed prototypes of trays and other packaging component designs. Shipper and Pallet Design: The structural designers at Sharp develop pallet layouts and shippers based on finished items to guarantee drug safety during distribution and storage. CR/SF Compliant Design and Testing: Sharp offers pharmaceutical contract packaging services and can determine the level of toxicity in child-friendly packaging. Various structural design services offered by Sharp include end-user interactions and compliance, child-resistant, senior-friendly (CR/SF) design, tamper evident features, multiple-component kitting requirements, and sustainable or specified materials. Additionally, Sharp’s graphic design capabilities include serialization artwork, brand identity, complete package graphics, product and package illustrations, and late-stage customization. Sharp’s broad range of tailored kitting options for medical devices, pharmaceuticals, and biotechnology calls for the packaging of multiple components into a single, self-contained unit. The design team at Sharp offers commercial packaging solutions and helps clients create a kit that best meets the end-user needs and product specifications. Its kitting services include labeling, tray packing, and boxing with comprehensive verification inspection to ensure the highest level of quality. How does Sharp manage the packaging of sterile formulations to ensure product integrity? Sharp has almost seven decades of packaging experience and it provides pharmaceutical packaging solutions for sterile and non-sterile formulations while maintaining the integrity and quality of products. It offers contract pharmaceutical packaging services and package design services from its US and EU facilities for injectables containing both small and large-volume batch sizes. For product launch and sample programs, its international design team works with clients to provide pharma packaging solutions and determine the optimal vial, prefilled syringe, and autoinjector packaging options. Through its partnership with Berkshire Sterile Manufacturing (BSM), Sharp also offers small-scale isolator-based sterile fill-finish options. It specializes in pharmaceutical clinical packaging and commercial packaging in cold chain storage, packaging in temperature and light-controlled environments, and specialty distribution for injectable drug products.  It also supports multi-country launches from the US and EU. Sharp has experience in parenteral and injectable format labeling and packaging such as vials, autoinjectors, syringes, and pens. Its specialized commercial and clinical services for injectables and parenterals include primary and secondary labeling of vials, IV bags, pre-filled syringes, and IV bottles in ambient, cold and ultra-cold environments, custom label generation, kitting, serialization and aggregation, and storage and distribution. Some of Sharp’s sterile packaging capabilities for injectable drug products include: Vial Labeling and Packaging: Sharp has decades of packaging experience and offers pharmaceutical packaging and labeling services for vials. Its contract packaging services include an automated visual inspection of labeling, tray and carton packing, cartoning of single and multipacks, tamper-evident solutions, cold-chain storage (2-8°C), and ultra-low temperature freezer banks (-20°C/-70°C). In addition to these services, Sharp provides package design, kitting, and segregated suites to handle highly potent APIs (HPAPI), cytotoxins, hormones, serialization and aggregation, and specialty distribution. Autoinjector and Pen Assembly, Labeling, and Packaging: Sharp excels in managing the complexities related to autoinjector or pen device labeling and packaging from its US and EU facilities. Moreover, its YpsoMate autoinjector device delivers a high level of technical accuracy required for the assembly of prefilled syringes into YpsoMate autoinjectors. Sharp’s experts also offer clinical trial packaging services and specialize in managing the challenges related to clinical trial logistics and packaging of biological formulations. Pre-Filled Syringe Assembly, Labeling, and Packaging: Sharp is a leader in the assembly, labeling, and packaging of pre-filled syringes and safety devices. It provides customized commercial and clinical pharma packaging services for both small and large-volume batch sizes for injectables. Small Scale Sterile Fill-Finish: Sharp partners with Berkshire Sterile Manufacturing (BSM) and offers high-quality, manufacturing, packaging, and distribution solutions for flexible fillers, BSM fills vials, cartridges, syringes, and lyophilization. Gene Therapy Clinical and Commercial Packaging: Sharp has over 70 years of experience in packaging complex pharmaceuticals such as low-volume, high-value gene therapies. Sharp is also engineered to provide demand-led supply commercial and clinical services including batch sizes as small as 1 vial, or packaging, labeling, and distribution in cold, ultra-cold, or cryogenic conditions. Sharp also has dedicated facilities in Bethlehem, PA, US, Heerenveen, and the Netherlands for handling gene therapies. These facilities are equipped with HEPA air handling systems, controlled temperature, humidity and dew point, full-sized -80°C freezer banks in dedicated production suites, constant monitoring of time-out-of-refrigeration, and specific freeze-thaw cycles. These facilities help in providing clinical trial packaging services and clinical secondary packaging solutions along with commercial packaging of sterile formulations. What range of pharmaceutical packaging solutions does Sharp offer for solid and liquid drug products? With a history spanning more than 70 years, Sharp is a pioneer in providing pharmaceutical packaging services that include primary and secondary packaging of solid, liquid, and semi-solid drug products for clinical and commercial scales from its state-of-the-art facilities. Sharp offers innovative and economical clinical packaging services for investigational medicinal products (IMP). It also supports the packaging of various dosage forms including bottling of solid formulations, and thermo and cold forming blister packaging for oral solids. Sharp also supports the packaging of powder and OSDs in sachets and pouches, oral and transdermal films in strips, and injectables in vials, syringes, and cartridges. Moreover, it is also involved in the packaging of semi-solids such as cream and ointment in tubes. Some of Sharp’s pharmaceutical packaging solutions for solid and liquid drug products are mentioned below: Bottle Packaging for Solids and Semi-solids: Sharp provides pharma packaging contract services for bottle packaging that include component sourcing, carton printing and in-line cartoning or bundling, comprehensive onsite engineering and validation support, serialization and aggregation, and strict quality control for packaged drugs. Sharp also offers high-quality nitrogen flush bottles and bottle packaging for moisture and oxygen-sensitive drugs. Blister Packaging for Oral Solids: Sharp provides various blister packaging solutions including thermoform and cold form blisters, patient packs, hospital unit dose packs, wallet cards, child-resistant lidding, sustainable foil and blister materials, and multiple products per blister. Apart from this, Sharp’s contract blister packaging services also involve multi-color foil printing, in-house tooling design and fabrication, polymer laminates (Aclar, PVC/PVDC, etc.) heat-seal coating resins, and automated visual inspection. Pouches and Sachets for Solids and Transdermal Patches (Primary and Secondary Packaging Services): Sharp has expertise in pouch and sachet packaging filled with solid dose, powder, thin film, and transdermal patch drug products. Sharp’s solid dose packaging solutions offer considerable pouch and sachet packaging backed by quality operations and project management knowledge. Sharp is home to a sizable assemblage of form, fill, and seal technologies. Based on decades of practical expertise, Sharp uses a wide range of innovative film structure materials, such as coated papers, high-barrier foils, and polymer laminates, and offers pharma packaging contract services. It also can support the production of multiple dosage forms for pharmaceutical products. Oral Thin Film and Transdermal Patches: Sharp provides primary and secondary packaging services for oral thin films and transdermal patches. Sharp specializes in die-cutting and pouching sublingual and oral dissolvable films, and transdermal drug delivery systems, and offers specialized pharmaceutical packaging services through quality procedures. It utilizes the most up-to-date solid dose packaging solutions and processes to safely package and safeguard specialty drug products. Sharp’s oral thin film and transdermal patch capabilities include highly accurate dosing by die-cutting laminated products to any size and shape, in-line printing of drug info, bar codes, lot number, expiration date, serialization with optical character verification (OCV), etc. Therefore, Sharp is a pharmaceutical contract packaging organization that offers clinical services, cold chain packaging, clinical packaging and labeling, and commercial packaging. Its pharmaceutical contract packaging service also encompasses primary and secondary clinical and commercial packaging. 

    Impressions: 347

    https://www.pharmacompass.com/pharma-blog/contract-packaging-primary-and-secondary-packaging-services-offered-by-sharp

    #LearnMore by PharmaCompass
    04 Mar 2024