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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: 639

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 Oct 2024: Lundbeck acquires Longboard for US$ 2.6 bn; molecular glue degrader tech witnesses dealmaking
In October, several pharma companies posted their third quarter (Q3) results. Drugmakers like Pfizer, BMS, Roche, Novartis, Sanofi, Merck and Incyte reported higher-than-expected Q3 earnings, beating analyst expectations. Despite these healthy results, pharma indices continued on their downward journey that had begun in September. The Nasdaq Biotechnology Index (NBI) dropped 2.6 percent from 4,771.85 to 4,650.07. The SPDR S&P Biotech ETF (XBI) fell 1.6 percent from 98.61 to 97.03, and the S&P Biotechnology Select Industry Index (SPSIBI) decreased 1.9 percent from 7,707.4 to 7,561.29.  Access the Pipeline Prospector Dashboard for October 2024 Newsmakers (Free Excel) Lundbeck buys Longboard, AbbVie picks up Aliada, Merck acquires Modifi in US$ 1 bn+ deals In mergers and acquisitions, Denmark’s Lundbeck agreed to buy California-based Longboard Pharmaceuticals for US$ 2.6 billion. The acquisition centers around bexicaserin, a promising phase 3 candidate for rare epilepsies including Dravet syndrome and Lennox-Gastaut syndrome, with Lundbeck projecting potential peak sales of US$ 1.5 billion to US$ 2 billion for this asset.  AbbVie acquired Boston-based Aliada Therapeutics for US$ 1.4 billion after reportedly outbidding at least three other drugmakers. The acquisition brings innovative blood-brain barrier technology to AbbVie’s portfolio, along with ALIA-1758, a phase 1 compound showing potential as a best-in-class therapy for Alzheimer’s disease. AbbVie also partnered with EvolveImmune Therapeutics in a potential US$ 1.4 billion deal (plus US$ 65 million upfront) to develop next-generation cancer biotherapeutics. The collaboration will leverage EvolveImmune’s innovative T-cell engager platform to create multispecific biologics targeting various oncology indications. Merck bolstered its oncology pipeline through the acquisition of Modifi Biosciences in a deal valued up to US$ 1.3 billion. The acquisition targets novel DNA modification therapeutics for challenging brain tumors, particularly glioblastomas. Merck  also entered into a potential US$ 1.9 billion deal with Mestag Therapeutics to explore fibroblast therapies for inflammatory diseases, leveraging Mestag’s innovative platform.  Access the Pipeline Prospector Dashboard for October 2024 Newsmakers (Free Excel) Pfizer, Novartis, Biogen sign molecular glue degrader deals; Astra in US$ 2 bn pact with CSPC There were at least three deals signed in October in the molecular glue degrader technology space. These degraders represent a novel therapeutic approach by facilitating the degradation of disease-causing proteins that are otherwise difficult to target with conventional drugs. First, Pfizer partnered Triana Biomedicines in a deal potentially exceeding US$ 1.5 billion, focusing on cancer applications. Second, Novartis committed US$ 150 million upfront to Monte Rosa Therapeutics in a deal worth up to US$ 2.25 billion. And Biogen tied up with Neomorph, pledging up to US$ 1.45 billion for neurological and immunological applications. Among other deals, AstraZeneca entered into a US$ 2 billion licensing agreement with CSPC Pharmaceutical Group for a novel lipid-lowering therapy, while Recordati acquired global rights to Sanofi’s Enjaymo for US$ 825 million upfront, with additional milestone payments of up to US$ 250 million. The Recordati-Sanofi deal focuses on cold agglutinin disease (CAD), a rare autoimmune disorder, and includes rights to sutimlimab, the first and only targeted therapy for CAD patients. Roche demonstrated its commitment to gene therapy advancement by expanding its collaboration with Dyno Therapeutics, committing over US$ 1 billion for adeno-associated virus (AAV) vector development, with an upfront payment of US$ 50 million. This expanded partnership builds on their initial 2020 collaboration and aims to accelerate the development of innovative gene therapies for neurological diseases.  Access the Pipeline Prospector Dashboard for October 2024 Newsmakers (Free Excel) AbbVie wins FDA nod for subcutaneous Parkinson’s drug; Roche med okayed for breast cancer October marked significant advances in the treatment of several major diseases. FDA approved AbbVie’s Vyalev for advanced Parkinson’s disease. This innovative therapy, utilizing foscarbidopa and foslevodopa prodrugs, delivers round-the-clock symptom control through subcutaneous infusion. The treatment represents a major advancement in managing motor fluctuations in late-stage patients, with market analysts projecting peak sales exceeding US$ 2 billion. In the oncology space, a historic milestone was reached with FDA’s approval of Vyloy, the world’s first therapy targeting CLDN18.2 proteins in gastric cancer. Developed by Astellas, the drug was approved for use in combination with chemotherapy for treating advanced gastric or gastroesophageal junction adenocarcinoma in adults with HER2-negative, CLDN18.2-positive tumors. This approval validates Astellas’ strategic US$ 1.4 billion acquisition of Ganymed Pharmaceuticals in 2016. Roche strengthened its position in breast cancer treatment with the approval of Itovebi, an oral PI3K inhibitor for first-line treatment of advanced hormone receptor-positive, HER2-negative breast cancer with PIK3CA mutation. This approval positions Itovebi as a strong competitor to existing treatments like Novartis' Piqray and AstraZeneca's Truqap, with Roche projecting annual peak sales of US$ 2.3 billion. Novartis expanded the reach of its leukemia treatment Scemblix through an accelerated approval for newly diagnosed Philadelphia chromosome-positive chronic myeloid leukemia in chronic phase. This expansion significantly increases the eligible patient population by approximately four times, building on its existing approval as a third-line treatment. Pfizer expanded its presence in the respiratory syncytial virus (RSV) market as FDA broadened the approval of Abrysvo to include at risk adults aged 18 to 50 years, making it the first and only RSV vaccine authorized for this population. In hematology, Pfizer secured approval for Hympavzi marking its second hemophilia approval in six months. This approval follows the earlier authorization of Pfizer’s one-time gene therapy Beqvez for hemophilia B in April. Iterum Therapeutics received FDA approval for its new oral antibiotic, Orlynvah, designed to treat uncomplicated urinary tract infections (uUTIs) in adult women who have limited or no alternative oral antibacterial treatment options. This marks the first US approval for an oral penem antibiotic.  Access the Pipeline Prospector Dashboard for October 2024 Newsmakers (Free Excel)  Gilead withdraws Trodelvy, J&J discontinues late-stage study of its bladder cancer candidate In a notable development for bladder cancer treatment, Gilead Sciences announced the withdrawal of Trodelvy from the US market after the targeted therapy, which received accelerated FDA approval in 2021 for metastatic urothelial cancer, failed to demonstrate survival benefits in a crucial confirmatory study.  Johnson & Johnson decided to discontinue the late-stage study of TAR-200, their investigational bladder cancer therapy, after interim analysis showed no superior benefits compared to standard chemo-radiation therapy. In neurology, Marinus Pharmaceuticals faced disappointment when their phase 3 trial of oral ganaxolone (Ztalmy) failed to meet its primary endpoint in reducing seizures associated with tuberous sclerosis complex (a genetic disorder). Marinus’ stock fell nearly 100 percent in October.  Access the Pipeline Prospector Dashboard for October 2024 Newsmakers (Free Excel)  Our view The last quarter was a good one for several drugmakers. Pfizer saw a surge in sales of its Covid drug Paxlovid to US$ 2.7 billion, encouraging it to up its guidance for Covid-related sales from US$ 8.5 billion to US$ 10.5 billion. For BMS, blockbusters like blood thinner Eliquis and cancer treatment Revlimid continued to bring in revenue. Merck’s growth was driven by the world’s top-selling drug, Keytruda, which saw revenue jump 17 percent compared to Q3 2023, beating analysts’ estimates. In a nutshell, the robust Q3 earnings of major pharma companies signals strong industry fundamentals, the volatility in pharma indices notwithstanding.  Access the Pipeline Prospector Dashboard for October 2024 Newsmakers (Free Excel)

Impressions: 4634

https://www.pharmacompass.com/pipeline-prospector-blog/pipeline-prospector-oct-2024-lundbeck-acquires-longboard-for-us-2-6-bn-molecular-glue-degrader-tech-witnesses-dealmaking

#PharmaFlow by PHARMACOMPASS
07 Nov 2024

WEEKLY NEWS RECAP #Phispers

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Lilly to acquire IBD drug developer Morphic for US$ 3.2 bn; Pfizer’s R&D chief to step down
This week saw Eli Lilly strike yet another deal as it announced the acquisition of Morphic Holding for about US$ 3.2 billion, thereby bolstering its position in the market for inflammatory bowel disease (IBD) drugs.Pfizer announced that its Chief Scientific Officer (CSO) Mikael Dolsten, a key figure behind the development of its Covid vaccine Comirnaty, will be stepping down after over 15 years with the drugmaker.A study found that Lilly’s glucagon-like peptide 1 (GLP-1) drug tirzepatide, used in its diabetes and weight-loss drugs Mounjaro and Zepbound, was more effective than its rival semaglutide, used in Novo Nordisk’s Ozempic and Wegovy, at shedding extra pounds.Another study found that GLP-1 drugs may have a role in preventing cancer. Meanwhile, a study undertaken by an American pharmacy found that only one in four patients in the US who were prescribed Novo Nordisk’s Wegovy or Ozempic for weight loss were still taking the popular medications after two years.Spain’s Grifols said it has received a takeover offer from its founding family and Brookfield Corporation to go private. The deal could potentially be worth about US$ 6 billion.Roche scrapped a trial testing its new immunotherapy tiragolumab in non-small cell lung cancer (NSCLC) patients after it failed to significantly improve survival more than a Keytruda-chemo combination. The Swiss drugmaker is reintroducing its eye therapy Susvimo in the US after voluntarily recalling it in October 2022.UniQure released promising 24-month data for its investigational gene therapy that showed AMT-130 significantly decreased disease progression in patients with Huntington’s disease.Lilly to acquire bowel disease drug developer Morphic for US$ 3.2 billionEli Lilly said it is acquiring Massachusetts-based Morphic Holding for approximately US$ 3.2 billion in cash, bolstering its presence in the US$ 26.65 billion IBD market. The Indiana drugmaker gains an investigational oral IBD therapy — MORF-057 — which will offer a more convenient dosing option compared to current injectable drugs, including Lilly’s Omvoh (mirikizumab). MORF-057 is being tested in three mid-stage studies to treat ulcerative colitis and Crohn’s disease, the two conditions that fall under IBD. Lilly sees the IBD space as a way to diversify beyond obesity.Pfizer’s R&D chief Mikael Dolsten, architect behind Comirnaty, to step downPfizer’s CSO Mikael Dolsten is stepping down after a 15-year career at the New York drugmaker. Under Dolsten, Pfizer won approvals for over 35 drugs and vaccines including for blockbuster drugs like its blood thinner Eliquis (apixaban), breast cancer med Ibrance (palbociclib), and heart disease treatment Vyndaqel (tafamidis meglumine). However, what stands out most is its Covid vaccine Comirnaty under Dolsten’s tenure. Jointly developed with BioNTech, the mRNA vaccine became the first Covid shot approved in the US. Comirnaty catapulted Pfizer’s sales to over US$ 100 billion in 2022.Lilly’s Mounjaro outperforms Novo’s Ozempic in weight loss studyElectronic records of over 18,000 obese or overweight US adults showed Lilly’s tirzepatide helped patients shed more weight than its rival Novo’s semaglutide, with the effect increasing over time. The study found that 82 percent of patients taking tirzepatide lost 5 percent of their starting body weight compared to 67 percent of those taking semaglutide, after a year. Novo pointed out that the analysis did not include its weight-loss drug Wegovy and said a head-to-head clinical trial is the best way to compare the two weight-loss drugs. Such a trial on tirzepatide and semaglutide is yet to conclude.GLP-1 drugs linked to lower cancer risk: Type 2 diabetes patients taking GLP-1 treatments “had a significant risk reduction” in developing 10 common types of cancers closely associated with obesity compared to those on insulin, according to a study published in JAMA Network Open. The study concluded that the “findings provide preliminary evidence of the potential benefit” of GLP-1 drugs for cancer prevention in high-risk populations.Few continue weight loss drugs after two years: Only one in four patients in the US who were prescribed Novo Nordisk’s Wegovy or Ozempic for weight loss were still taking the popular medications two years later, a Reuters report said. The analysis, undertaken by an American pharmacy, does not include details about why patients quit. Another news report said only about 15 percent of people who began taking GLP-1 drugs such as Wegovy stuck with them after two years.Grifols gets US$ 6 billion takeover offer from founding family, BrookfieldSpanish multinational pharmaceutical company Grifols said it is evaluating a takeover offer from its founding family and the Canadian investment management company Brookfield that would delist the company from the Spanish and Nasdaq stock markets. Based on the company’s current market value, the deal is potentially worth around US$ 6 billion. The Grifols family holds a stake of about 30 percent, which they don’t plan to sell. Brookfield is mulling investing over € 5 billion (US$ 5.41 billion), part of which will be to refinance and restructure the company’s debt. The beleaguered drugmaker was rocked by allegations of fraud earlier this year over manipulation of its debt.FDA rejects Novo’s weekly insulin, seeks manufacturing informationFDA has issued Novo Nordisk a complete response letter (CRL), declining to approve the Danish drugmaker’s weekly insulin Awiqli (insulin icodec). The agency has requested information related to the manufacturing process and the type 1 diabetes indication before the review of the application can be completed, a company statement said. In May, an FDA panel had voted seven to four against the benefits of Awiqli outweighing its risks.Roche scraps trial after new immunotherapy loses to Keytruda-chemo comboRoche is putting an end to a trial testing its new immunotherapy tiragolumab in non-small cell lung cancer (NSCLC) patients. Tiragolumab is part of a new class of drugs called anti-TIGIT antibodies. The study involving 524 patients with NSCLC tested tiragolumab in combination with Roche’s Tecentriq (atezolizumab) in the first line setting. It failed to best Merck’s Keytruda (pembrolizumab) plus chemotherapy as a first line of treatment in the phase 2/3 study.Meanwhile, Roche is reintroducing Susvimo (ranibizumab injection) in the US after voluntarily recalling it in October 2022. The implant used to treat patients with neovascular age-related macular degeneration (wet AMD) requires a one-time surgery to be inserted into the eye.UniQure posts strong data on gene therapy for Huntington’s diseaseUniQure released promising 24-month data for its investigational gene therapy that showed AMT-130 significantly decreased disease progression in patients with Huntington’s disease. The early-mid stage data showed that among 29 US and European patients, those given the higher dose showed an 80 percent reduction of the neurodegenerative disease progressing, while those given the lower dose saw a 30 percent reduction of the same.  

Impressions: 1367

https://www.pharmacompass.com/radio-compass-phisper/lilly-to-acquire-ibd-drug-developer-morphic-for-us-3-2-bn-pfizer-s-r-d-chief-to-step-down

#Phispers by PHARMACOMPASS
11 Jul 2024

NEWS #PharmaBuzz

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https://www.reuters.com/business/healthcare-pharmaceuticals/bristol-myers-posts-higher-than-expected-quarterly-profit-blood-thinner-cancer-2026-04-30/

REUTERS
30 Apr 2026

https://firstwordpharma.com/story/7206236

FIRSTWORD PHARMA
24 Apr 2026

https://www.biospace.com/business/bms-beats-again-despite-eliquis-and-cobenfy-disappointments

BIOSPACE
05 Feb 2026

https://www.businesswire.com/news/home/20251219775505/en/Bristol-Myers-Squibb-Announces-Agreement-with-U.S.-Government-to-Improve-Affordability-and-Access-to-Critical-Medicines-for-Americans

BUSINESSWIRE
19 Dec 2025

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=210108

FDA
04 Nov 2025

https://www.indianpharmapost.com/news/taho-pharma-submits-nda-to-fda-for-worlds-first-apixaban-oral-dissolving-film-17944

INDPHARMAPOST
06 Oct 2025