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DATA COMPILATION #PharmaFlow

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Top Pharma Companies & Drugs in 2025: Lilly vaults eight spots to emerge at the top; GLP-1 drugs dominate list
For the pharmaceutical industry, 2025 was a watershed year when obesity drugs settled firmly in the mainstream market. Glucagon-like peptide-1 (GLP-1) receptor agonists that treat diabetes and help in weight loss, dominated our top 10 list of drugs with four entries — Mounjaro (tirzepatide), Ozempic (semaglutide), Zepbound (tirzepatide) and Wegovy (semaglutide).In 2024, the top 10 drugs generated a total revenue of US$ 142 billion. This figure rose significantly in 2025, climbing to US$ 180.02 billion, reflecting strong growth.The year unequivocally belonged to Eli Lilly. The Indiana-headquartered drugmaker made a dramatic ascent, leaping from the ninth spot in 2024 to the numero uno position in our top drugmakers’ list for 2025. It posted 45 percent growth in sales, which rose to US$ 65.18 billion in 2025.In terms of therapeutic areas, oncology saw the maximum sales (at US$ 229.1 billion), followed by immunology (US$ 126.8 billion), infectious diseases (US$ 99.2 billion), diabetes (US$ 95.8 billion), neurology (US$ 70.4 billion), cardiology (US$ 67.6 billion) and hematology (US$ 29.3 billion). View Our Interactive Dashboard on Top Drugs in 2025 by Sales (Free Excel Available)Lilly zooms past Pfizer on back of tirzepatide franchise; Roche, AbbVie, J&J make it to top five Eli Lilly’s spectacular climb to the number one spot was driven by Mounjaro and Zepbound. Mounjaro leapt from the eighth spot in 2024 (when its sales stood at US$ 11.5 billion) to the number two position in 2025, raking in US$ 23 billion. Lilly’s other GLP-1 drug, Zepbound, also broke into the top 10, debuting at number nine with sales of US$ 13.5 billion. Taken together, Lilly’s tirzepatide franchise hit US$ 36.50 billion in 2025, surpassing Merck's Keytruda (pembrolizumab).At the number two position was Pfizer, with sales of US$ 62.58 billion. Notably, not a single Pfizer drug made it to the top 10 list. Pfizer’s sales fell by 1.63 percent in 2025, from US$ 63.63 billion in 2024. The decline was attributed to lower Covid‑19 revenues due to reduced infection rates, which impacted Paxlovid (nirmatrelvir/ritonavir) sales, and a narrower US vaccine recommendation, which affected Comirnaty (tozinameran) sales.Roche came third, reporting sales of CHF 47.7 billion  (US$ 62.10 billion) in 2025, compared to CHF 46.2 billion (US$ 50.86 billion) in 2024.At number four was AbbVie — it reported full-year net revenues of US$ 61.16 billion in 2025, compared to US$ 56.33 billion in 2024. The company’s immunology portfolio remained a key driver, bringing in US$ 30.41 billion in sales. Skyrizi (risankizumab) — approved for plaque psoriasis, psoriatic arthritis, Crohn’s disease, and ulcerative colitis — emerged as a major growth engine, with sales of US$ 17.56 billion.Rounding out the top five was Johnson & Johnson, whose innovative medicine division reported sales of US$ 60.4 billion, up from US$ 56.9 billion in 2024. View Our Interactive Dashboard on Top Drugs in 2025 by Sales (Free Excel Available)Merck’s Keytruda retains top-selling drug status, followed by Lilly’s Mounjaro, Novo’s OzempicMerck’s Keytruda retained its position as the world’s best-selling drug for the third consecutive year, generating approximately US$ 31.6 billion in sales, up from US$ 29.5 billion in 2024 and US$ 25 billion in 2023. Keytruda has become the pillar of cancer immunotherapy, with over 40 indications. The launch of Keytruda Qlex, a subcutaneous formulation co-administered with berahyaluronidase alfa, has further strengthens its lifecycle.Amongst other oncology drugs, J&J’s Darzalex (daratumumab) generated US$ 14.4 billion in sales, taking it to the number seven spot. Its strong performance has been supported by Darzalex Faspro, a subcutaneous formulation launched in 2020 that significantly reduces administration time. Growth from Darzalex and other brands helped offset the decline in Stelara (ustekinumab), whose sales fell 41 percent to US$ 6.1 billion, from US$ 10.4 billion in 2024.Among diabetes, obesity and metabolic drugs, Lilly’s Mounjaro was at the number two spot,  followed by Novo Nordisk’s Ozempic at number three. Ozempic posted sales of US$ 20.09 billion. Lilly’s Zepbound was at the ninth spot, with sales of US$ 13.54 billion. Novo’s Wegovy was tenth, with sales of US$ 12.5 billion. Together with Rybelsus, Novo’s semaglutide franchise generated approximately US$ 36.1 billion in 2025 sales.In immunology, Sanofi and Regeneron’s Dupixent (dupilumab) stood fourth and maintained its leadership with sales of US$ 18.6 billion. Dupixent is now approved across nine indications.At fifth position was another immunology drug — AbbVie’s Skyrizi (risankizumab). It has emerged as AbbVie’s key growth engine post‑Humira (adalimumab), delivering 49.87 percent growth and generating US$ 17.56 billion in 2025 sales. First approved in April 2019 for plaque psoriasis, it is now approved across four indications.The other drugs in our top 10 list were Eliquis (apixaban) and Biktarvy (bictegravir/emtricitabine/tenofovir alafenamide). Eliquis, co-developed and commercialized by Bristol Myers Squibb and Pfizer, stood sixth with sales of US$ 14.4 billion. Gilead’s Biktarvy (bictegravir/emtricitabine/tenofovir alafenamide) held the number eight position, with sales of US$ 14.3 billion in 2025. The drug commands over 52 percent of the US market for HIV treatments. View Our Interactive Dashboard on Top Drugs in 2025 by Sales (Free Excel Available)Astra’s revenue rises by 8.6 percent; Merck, Novartis, Sanofi, Novo make it to top 10 AstraZeneca’s revenues increased 8.6 percent to US$ 58.73 billion, compared to US$ 54.10 billion in 2024, though its ranking fell from fifth to sixth position in 2025. Astra’s revenue growth was driven by strong performance across oncology, cardiovascular, renal and metabolism, respiratory and immunology, and rare disease portfolios. Farxiga (dapagliflozin), a drug used to manage blood sugar, was a key driver, generating US$ 8.4 billion in revenue in 2025.At number seven was Merck, with sales of US$ 58.1 billion, reflecting a modest growth of 1.3 percent, which was driven by Keytruda.Novartis stood eighth on our 2025 list (against seventh in 2024), with net sales of US$ 54.5 billion in 2025, up from US$ 50.3 billion in 2024. Sanofi landed at the ninth position, with sales of US$ 51.7 billion, against US$ 42.6 billion in 2024. Novo Nordisk rounded out the top ten, posting revenues of DKK 309.06 bn (US$ 48.7 billion) in 2025 — a growth of 21.37 percent compared to DKK 290.40 billion (US$ 40.2 billion) in 2024 — driven primarily by its obesity and diabetes care portfolio. View Our Interactive Dashboard on Top Drugs in 2025 by Sales (Free Excel Available)Our viewThe 2025 rankings confirm what analysts have been expecting for some time — that the market for anti-obesity drugs could reach US$ 100 billion by 2030. The four GLP-1 drugs in our 2025 list together generated combined revenue of approximately US$ 70 billion. At this pace, the US$ 100 billion market size may arrive sooner than projected, perhaps as early as 2026 or 2027.

Impressions: 610

https://www.pharmacompass.com/radio-compass-blog/top-pharma-companies-drugs-in-2025-lilly-vaults-eight-spots-to-emerge-at-the-top-glp-1-drugs-dominate-list

#PharmaFlow by PHARMACOMPASS
11 Jun 2026

STOCK RECAP #PipelineProspector

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Pipeline Prospector April-May 2026 highlights: Sun Pharma buys Organon for about US$ 11.8 bn; Lilly on acquisition overdrive
April and May were tough months, with oil prices rising globally due to the war in the Middle East. Yet, the world of pharmaceuticals continued to witness large M&A deals and collaborations.A highlight was the slew of deals signed with artificial intelligence firms — Bristol Myers Squibb (BMS) signed a strategic agreement with Anthropic to deploy Claude Enterprise across its entire global operations; Eli Lilly signed a DNA editing deal worth up to US$ 2.25 billion with AI-driven firm Profluent Bio; and Merck partnered with Google Cloud to enhance its digital backbone as an AI-enabled enterprise.The indices continued to inch upwards. The Nasdaq Biotechnology Index (NBI) increased from 5,819.43 at the end of April to 5,989.81 at the end of May. The SPDR S&P Biotech ETF increased from 130.62 to 136.69. The S&P Biotechnology Select Industry Index (SPSIBI) increased from 10,262.80 to 10,689.60. Meanwhile, the S&P 500 increased from 7,234.54 to 7,580.06. Access the Pipeline Prospector Dashboard for May 2026 Newsmakers (Free Excel)Lilly on acquisition overdrive: buys Kelonia for up to US$ 7 bn, three vaccine makers for US$ 3.8 bn Buoyed by the success of its obesity drugs Zepbound (tirzepatide) and Foundayo (orforglipron), Eli Lilly has been on a shopping spree. So far, Lilly has made 10 acquisitions in 2026.In April, Lilly acquired clinical-stage biotech, Kelonia Therapeutics, for up to US$ 7 billion, and Ajax Therapeutics for up ‌to US$ 2.3 billion in cash. Privately-held Kelonia is pioneering cancer treatments such as in vivo gene delivery. Ajax’s lead asset, AJ1-11095, is an investigational drug currently in early-stage clinical trials for the treatment of rare blood cancers.In May, Lilly announced an additional US$ 4.5 billion investment across two of its manufacturing sites in Lebanon, Indiana, bringing its total commitments in this American state to more than US$ 21 billion since 2020. Last week, Lilly announced agreements to acquire three vaccine companies — Curevo Inc, LimmaTech Biologics, and Vaccine Company —  in deals worth up to US$ 3.8 billion. Access the Pipeline Prospector Dashboard for May 2026 Newsmakers (Free Excel)FDA approves Astra’s new hypertension treatment; okays AbbVie’s rare blood cancer drugIn May, the US Food and Drug Administration (FDA) approved AstraZeneca’s Baxfendy (baxdrostat), a first-in-class treatment for hypertension to be used in combination with other antihypertensive medications.Additionally, FDA granted two new approvals to AstraZeneca and Daiichi Sankyo’s Enhertu (trastuzumab deruxtecan) for treating early-stage HER2-positive breast cancer. The drug has now been approved for use before surgery (to shrink tumors) and after surgery (to reduce the risk of recurrence). Enhertu is already approved for treating advanced breast cancer.The agency approved Arvinas and Pfizer’s Veppanu (vepdegestrant) for the treatment of an advanced type of breast cancer known as estrogen receptor-positive/human epidermal growth factor receptor 2-negative, estrogen receptor 1-mutated advanced or metastatic breast cancer. The agency also approved AbbVie’s Decnupaz (pivekimab sunirine-pvzy) for the treatment of adult patients with blastic plasmacytoid dendritic cell neoplasm, an aggressive and ultra-rare blood cancer.In April, FDA granted accelerated approval to Regeneron Pharmaceuticals’ Otarmeni (lunsotogene parvec-cwha) for the treatment of a rare genetic form of hearing loss caused by a faulty gene. The agency also approved Merck’s Idyvnso, a new, two-drug single-tablet regimen of doravirine and islatravir, for treating HIV-1 infections in adults. Access the Pipeline Prospector Dashboard for May 2026 Newsmakers (Free Excel)Sun Pharma acquires Organon for ~US$ 11.8 bn; Gilead buys Tubulis for up to US$ 5 bnApril and May saw several big and mid-size M&A deals. Sun Pharmaceutical Industries made the largest overseas acquisition by an Indian drugmaker in April, as it acquired New Jersey-based Organon in an all-cash deal valued at about US$ 11.75 billion, including debt.Gilead announced the acquisition of Germany-based clinical-stage biotech Tubulis GmbH in early April for up to US$ 5 billion to strengthen its cancer drugs pipeline. With this acquisition, Gilead will gain access to Tubulis’ next-generation antibody-drug conjugates (ADCs).In the first week of May, Rome-based Angelini Pharma announced the acquisition of American rare-disease drug maker Catalyst Pharmaceuticals for €3.5 billion (US$ 4.1 billion). Additionally, Neurocrine Biosciences acquired Soleno Therapeutics for US$ 2.9 billion in cash. The deal gives Neurocrine access to Vykat XR (diazoxide choline), the first drug approved in the US to treat a rare genetic disorder known as hyperphagia. And Italy’s Chiesi Group announced the acquisition of US-listed KalVista Pharmaceuticals in an all-cash deal valued at about US$ 1.9 billion. The acquisition will strengthen Chiesi’s rare diseases strategy. Access the Pipeline Prospector Dashboard for May 2026 Newsmakers (Free Excel)China’s Hengrui in up to US$ 15.2 bn deal with BMS, Innovent in oncology tie-up with PfizerLast month, China’s Jiangsu Hengrui Medicine struck global ‌collaboration and licensing deals with BMS that include an upfront payment of US$ 600 million and potential milestone payments of up to US$ 15.2 billion. The deal covers ‌four cancer and blood-disease drug candidates from Hengrui, four immunology candidates from BMS and five additional projects the companies will work on together.Last week, Innovent Biologics and Pfizer entered into a strategic global licensing and collaboration agreement worth up to US$ 10.5 billion to develop 12 early-stage cancer medicines.In April, Australia’s Telix Pharmaceuticals entered into a collaboration with Regeneron Pharmaceuticals to jointly develop and commercialize next-generation radiopharmaceutical therapies. Telix will receive US$ 40 million upfront and earn up to US$ 2.1 billion in milestone payments and royalties. Access the Pipeline Prospector Dashboard for May 2026 Newsmakers (Free Excel)Celcuity’s therapy beats Novartis’ Piqray in breast cancer trial; Moderna’s mRNA flu scores late-stage win US biotech Celcuity announced positive results from a large phase 3 trial testing its experimental drug gedatolisib in patients with a HR-positive, HER2-negative breast cancer who carry a mutation in the PIK3CA gene and whose cancer had worsened despite earlier treatment.Moderna’s mRNA flu vaccine (mRNA-1010) outperformed the standard flu shot in a phase 3 trial, with the mRNA shot performing about 27 percent better.Merck’s experimental drug sacituzumab tirumotecan, developed in collaboration with China’s Kelun-Biotech, showed positive results in a late-stage trial in certain patients with advanced or recurrent endometrial cancer, a type of uterine cancer.In April, there was also news that Novo Nordisk’s experimental oral drug etavopivat successfully met two co-primary endpoints in a late-stage trial on adults and adolescents with sickle cell disease, a debilitating, life-threatening disease. And AstraZeneca’s ‌experimental treatment tozorakimab showed benefit in reducing moderate-to-severe exacerbations of chronic obstructive pulmonary disease (COPD) in a late-stage trial. Access the Pipeline Prospector Dashboard for May 2026 Newsmakers (Free Excel)Our viewDespite macroeconomic and geopolitical headwinds, pharmaceutical companies have continued to expand through acquisitions, deals, and collaborations. AI is bringing about a structural shift and becoming central to competitive strategy. Overall, the sector is not only weathering global uncertainty, but actively reshaping itself for the next phase of growth.

Impressions: 592

https://www.pharmacompass.com/pipeline-prospector-blog/pipeline-prospector-april-may-2026-highlights-sun-pharma-buys-organon-for-about-us-11-8-bn-lilly-on-acquisition-overdrive

#PharmaFlow by PHARMACOMPASS
04 Jun 2026

WEEKLY NEWS RECAP #Phispers

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Gilead buys Arcellx for US$ 7.8 billion; FDA approves Vanda’s antipsychotic pill for bipolar disorder, schizophrenia
In this week’s news, Gilead Sciences has entered into an agreement to acquire its cancer therapy partner Arcellx for US$ 7.8 billion. Gilead’s cell therapy subsidiary — Kite Pharma — has been working with Arcellx since 2022 on an investigational CAR T-cell therapy, which is the centerpiece of this deal.Novo Nordisk has entered into a US$ 2.1 billion deal with privately-held Vivtex Corp to develop next-generation oral drugs for obesity and diabetes. GSK has struck an up to US$ 1 billion licensing deal with Frontier Biotechnologies to obtain exclusive worldwide rights to develop, manufacture, and commercialize two small interfering RNA (siRNA) pipeline products that target kidney diseases. And Astellas Pharma has entered into global strategic collaboration with Vir Biotechnology to advance a treatment for prostate cancer. The deal is worth up to US$ 1.7 billion.The week saw several approvals granted by the US Food and Drug Administration (FDA). The agency approved Vanda Pharmaceuticals’ Bysanti (milsaperidone), a first-line therapy for acute bipolar I disorder and schizophrenia in adults. The agency also granted full approval to Pfizer’s Braftovi (encorafenib) in combination with Erbitux (cetuximab) and fluorouracil-based chemotherapy for the treatment of adult patients with a type of metastatic colorectal cancer (mCRC). The combo therapy had received accelerated approval in 2024.FDA granted Sanofi and Regeneron’s Dupixent its ninth approval — this time to treat adult and pediatric patients aged six years and older with a chronic inflammatory condition known as allergic fungal rhinosinusitis (AFRS).FDA also approved another combination regimen — of AbbVie’s Venclexta (venetoclax) and AstraZeneca’s Calquence (acalabrutinib) — for the treatment of previously untreated adult patients with chronic lymphocytic leukemia (CLL). And Eton Pharmaceuticals’ liquid therapy — Desmoda (desmopressin) — for the management central diabetes insipidus also clinched an FDA approval.Gilead buys Arcellx for US$ 7.8 billion for its multiple myeloma CAR-T therapyGilead Sciences has entered into an agreement to acquire its cancer therapy partner Arcellx for US$ 7.8 billion. The two companies have been in a cell therapy development collaboration since 2022 through Kite Pharma, Gilead’s cell therapy subsidiary. Kite has been co-developing and co-commercializing Arcellx’s lead candidate anitocabtagene autoleucel (anito-cel), an investigational CAR T-cell therapy for patients with multiple myeloma. Anito-cel is the centerpiece of this deal.FDA approves Vanda’s antipsychotic pill for bipolar I disorder, schizophreniaFDA has approved Vanda Pharmaceuticals’ Bysanti (milsaperidone) tablets, a first-line therapy for two mental health conditions — acute bipolar I disorder and schizophrenia. Bysanti is a new chemical entity (NCE), and an atypical antipsychotic. It works by blocking dopamine and serotonin receptors in the brain, which help regulate mood, stress, delusions, and alertness. This is the third FDA approval won by the company in recent months.Dupixent okayed for allergic fungal rhinosinusitis: FDA has approved Sanofi and Regeneron’s Dupixent (dupilumab) for the treatment of adult and pediatric patients aged six years and older with allergic fungal rhinosinusitis (AFRS) who have a history of sino-nasal surgery. This is Dupixent’s ninth FDA approval. AFRS is a chronic inflammatory condition that can cause nasal polyps, persistent congestion, thick mucus, and loss of smell. FDA evaluated Dupixent under priority review for the treatment of AFRS, and it is the first treatment approved for the condition. Novo inks up to US$ 2.1 bn deal with Vivtex for its next-gen obesity, diabetes drugsEarlier this week, there was news that Novo Nordisk’s next-generation obesity drug CagriSema (cagrilintide and semaglutide) underperformed Eli Lilly’s Zepbound (tirzepatide) in a head-to-head trial. Novo didn’t let the setback weigh it down. It quickly struck an up to US$ 2.1 billion deal with privately-held American company Vivtex Corp to develop next-generation oral drugs for obesity and diabetes. Under the partnership, Vivtex will license some of its oral drug-delivery technology, while Novo Nordisk will take charge of global development and commercialization. The deal covers research funding, milestone payments, and tiered royalties on product sales.Frontier strikes up to US$ 1 billion deal with GSK: Frontier Biotechnologies has struck an exclusive licensing agreement with GSK. Under the terms of the agreement, GSK will obtain exclusive worldwide rights to develop, manufacture, and commercialize two of Frontier Biotechnologies’ small interfering RNA (siRNA) pipeline products that target kidney diseases.Astellas ties up with Vir Biotech: Astellas Pharma has entered into global strategic collaboration with Vir Biotechnology to advance a T-cell engager targeting prostate-specific membrane antigen (PSMA) and CD3 proteins for the treatment of prostate cancer. The deal involves an upfront payment, milestone payments and royalties that could together add up to US$ 1.7 billion.FDA okays Venclexta-Calquence combo for untreated chronic lymphocytic leukemiaAbbVie has said FDA has approved a supplemental new drug application (sNDA) for the combination regimen of Venclexta (venetoclax) and AstraZeneca’s Calquence (acalabrutinib) for the treatment of previously untreated adult patients with chronic lymphocytic leukemia (CLL). Venclexta is manufactured by AbbVie and Genentech (a member of the Roche group).Pfizer’s Braftovi combo regimen gets full approval: FDA has granted full approval to Braftovi (encorafenib) in combination with Erbitux (cetuximab) and fluorouracil-based chemotherapy for the treatment of adult patients with a type of metastatic colorectal cancer. The combo therapy had received accelerated approval in 2024.FDA approves Eton’s liquid therapy for managing central diabetes insipidusFDA has okayed Eton Pharmaceuticals’ liquid therapy  — Desmoda (desmopressin) — for the management of a rare hormonal disorder, known as arginine vasopressin deficiency (AVP-D), or central diabetes insipidus. In AVP-D, patients lack the hormone that regulates water balance, causing excessive urination and thirst. This is the first-of-its-kind liquid therapy for AVP-D.Zepbound KwikPen okayed: FDA has approved a label expansion for Eli Lilly’s Zepbound (tirzepatide) to include the four-dose single-patient-use KwikPen that delivers a full month of treatment in one device. Rival Novo Nordisk has been selling its weight loss drug Wegovy (semaglutide) as a single-dose weekly auto-injector pen in the US since 2021.Gossamer’s pulmonary arterial hypertension drug fails late-stage trialGossamer Bio’s experimental treatment seralutinib, which is an inhaled drug, failed to significantly improve exercise capacity in patients with the rare lung condition known as pulmonary arterial hypertension (PAH) in a late-stage study. PAH is caused by constriction of the arteries in the lungs, which leads to high blood pressure.FDA proposes framework to speed up personalized gene therapy approvalsFDA has proposed a new framework to speed up approvals of personalized treatments for rare and life-threatening genetic diseases. It offers clearer rules for drugmakers to develop genome-editing and RNA-based drugs while requiring them to justify why randomized controlled trials are not feasible.

Impressions: 957

https://www.pharmacompass.com/radio-compass-phisper/gilead-buys-arcellx-for-us-7-8-billion-fda-approves-vanda-s-antipsychotic-pill-for-bipolar-disorder-schizophrenia

#Phispers by PHARMACOMPASS
26 Feb 2026

NEWS #PharmaBuzz

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https://www.accessnewswire.com/newsroom/en/healthcare-and-pharmaceutical/cvs-caremark-delivers-affordability-and-access-to-glp-1-weight-manage-1174950

ACCESSWIRE
10 Jun 2026

https://www.prnewswire.com/news-releases/zepbound-tirzepatide-and-shaquille-oneal-launch-national-campaign-after-nba-legend-learns-the-obstructive-sleep-apnea-he-has-lived-with-for-years-is-treatable-302795901.html

PR NEWSWIRE
10 Jun 2026

https://www.business-standard.com/industry/news/india-s-glp-1-market-enters-slower-growth-phase-after-semaglutide-surge-126060801024_1.html

BUSINESS STD
08 Jun 2026

https://www.prnewswire.com/news-releases/lillys-oral-glp-1-foundayo-orforglipron-delivered-superior-a1c-control-and-weight-loss-in-three-pivotal-type-2-diabetes-trials-302793407.html

PR NEWSWIRE
08 Jun 2026

https://www.globenewswire.com/news-release/2026/06/08/3307960/0/en/mitorx-therapeutics-presents-promising-preclinical-data-on-mtrx31-a-mitochondrial-targeted-small-molecule-for-metabolically-unhealthy-obesity-at-the-american-diabetes-association-s.html

GLOBENEWSWIRE
08 Jun 2026

https://www.prnewswire.com/news-releases/lillys-foundayo-orforglipron-the-only-oral-glp-1-taken-without-food-or-water-restrictions-was-associated-with-significant-weight-loss-in-women-at-every-stage-of-menopause-302793332.html

PR NEWSWIRE
07 Jun 2026