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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: 674

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 February 2026 highlights: Gilead buys Arcellx for US$ 7.8 bn; FDA okays Vanda’s psychotic pill
February was a month of upheavals. In the US, the Supreme Court ruled that President Donald Trump exceeded his authority by imposing broad tariffs. Soon after the ruling, Trump imposed a temporary 15 percent global tariff under a separate trade law. The month ended with the US and Israel launching a major military operation against Iran, and the region now appears headed for a prolonged conflict.Despite the turbulent geopolitical environment, the biotech indices continued to grow steadily. The Nasdaq Biotechnology Index (NBI) rose 3.68 percent, moving from 5,852.67 to 6,041.31. The SPDR S&P Biotech ETF (XBI) gained 2.4 percent, rising from 124.75 to 127.27, and the S&P Biotechnology Select Industry Index (SPSIBI) increased 2.4 percent, rising from 9,746.25 to 9,954.51. In comparison, the S&P 500 fell by 0.55 percent — from 6,916.64 to 6,878.88.  Access the Pipeline Prospector Dashboard for February 2026 Newsmakers (Free Excel)Gilead buys Arcellx for US$ 7.8 billion; Lilly acquires Orna for its circular RNA therapeutics The month’s biggest acquisition was made by Gilead Sciences, which acquired its cancer therapy partner Arcellx for US$ 7.8 billion. The two companies have been collaborating on cell therapy development since 2022 through Kite Pharma, Gilead’s subsidiary. The centerpiece of the deal is Arcellx’s investigational CAR-T therapy for multiple myeloma — anitocabtagene autoleucel.Eli Lilly announced the acquisition of Orna Therapeutics for up to US$ 2.4 billion in cash. The deal will give Lilly access to a new class of therapeutics, known as circular RNA, that allows patients’ own cells to generate therapies (to treat underlying diseases) inside the body, doing away with the need for cell extraction.Among other deals, GSK acquired Canadian biotech 35Pharma for US$ 950 million in cash. The acquisition includes HS235, an investigational therapy being studied for pulmonary arterial hypertension (PAH) and pulmonary hypertension associated with heart failure with preserved ejection fraction. GSK’s stock was up 14 percent in February.  Access the Pipeline Prospector Dashboard for February 2026 Newsmakers (Free Excel)FDA approves Vanda’s antipsychotic pill Bysanti; Dupixent okayed for allergic fungal rhinosinusitisThe month saw several key approvals. The US Food and Drug Administration (FDA) approved Vanda Pharmaceuticals’ Bysanti (milsaperidone) tablets, a first-line therapy for acute bipolar I disorder and schizophrenia. This marks the company’s third FDA approval in recent months.The agency also approved Sanofi and Regeneron’s Dupixent (dupilumab) for the treatment of adults and pediatric patients with allergic fungal rhinosinusitis (AFRS) who have a history of sino-nasal surgery. AFRS is a chronic inflammatory condition that can cause nasal polyps, persistent congestion, and loss of smell. This is Dupixent’s ninth FDA approval.Merck’s Keytruda (pembrolizumab) and Keytruda Qlex (pembrolizumab and berahyaluronidase alfa-pmph) in combination with paclitaxel, with or without bevacizumab, were approved for treating a form of ovarian cancer. This marks Keytruda’s first FDA approval in ovarian cancer.Pfizer’s Braftovi (encorafenib) was granted full approval when used in combination with Erbitux (cetuximab) and fluorouracil-based chemotherapy to treat adults with a type of metastatic colorectal cancer. The combo therapy had received accelerated approval in 2024.FDA also approved AbbVie’s supplemental new drug application 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.  Access the Pipeline Prospector Dashboard for February 2026 Newsmakers (Free Excel)Lilly in another oncology deal with Innovent worth up to US$ 8.85 bn; Novo inks obesity deal with VivtexLilly entered into a strategic collaboration with Chinese drugmaker Innovent Biologics to advance novel medicines in oncology and immunology. This is the seventh collaboration between the two drugmakers. Lilly will pay US$ 350 million upfront and as much as US$ 8.5 billion in milestone payments.Madrigal Pharmaceuticals entered into a global license agreement with Suzhou Ribo Life Science and its subsidiary Ribocure Pharmaceuticals for six preclinical small interfering RNA programs targeting metabolic dysfunction-associated steatohepatitis (MASH). Madrigal will pay US$ 60 million upfront and US$ 4.4 billion in milestone payments.Novo Nordisk has inked a deal worth up to US$ 2.1 billion with privately-held American company Vivtex Corp to develop next-generation oral drugs for obesity and diabetes.Astellas Pharma (stock up 16 percent) has entered into a global strategic collaboration with Vir Biotechnology to advance a T-cell engager targeting prostate-specific membrane antigen 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.There were also a few AI deals. Takeda Pharmaceutical has entered into a multi-year partnership that could be worth over US$ 1.7 billion with San Diego-headquartered Iambic to use AI to design small-molecule drugs for cancer and gastrointestinal diseases. And, Novartis (stock up 13 percent in February) signed a research collaboration and licensing deal worth up to US$ 1.8 billion with American biotech Unnatural Products (UNP) to develop therapeutics with potential applications in cardiovascular diseases. Novartis will license UNP’s AI-enhanced macrocycle platform.  Access the Pipeline Prospector Dashboard for February 2026 Newsmakers (Free Excel)Roche’s Gazyva scores phase 3 win in rare autoimmune kidney disorder; Novo’s CagriSema beats WegovyIn a phase 3 trial, Roche’s Gazyva (obinutuzumab) met its primary endpoint, holding the potential to become the first approved therapy for primary membranous nephropathy, a rare autoimmune kidney disorder. According to top-line results, significantly more patients achieved complete remission at two years with Gazyva, compared to immunosuppressant tacrolimus. Novo Nordisk said its experimental next-generation weight-loss drug CagriSema (cagrilintide and semaglutide) delivered greater reductions in body weight and blood sugar than its blockbuster Wegovy (semaglutide) in a late-stage trial in patients with type 2 diabetes. Novo has positioned CagriSema as a successor to Wegovy and a potential rival to Eli Lilly’s Zepbound (tirzepatide).Eli Lilly’s Retevmo (selpercatinib), an FDA-approved drug for lung and thyroid cancers that have RET gene alterations, has demonstrated statistically significant improvement in event-free survival in patients with early-stage (2-3A) RET fusion-positive non-small cell lung cancer.In a phase 3 trial, Bayer’s experimental blood thinner — asundexian — reduced the risk of recurrence of stroke by 26 percent. And Compass Pathways’ psilocybin-based therapy — COMP360 — eased symptoms in treatment-resistant depression. This is the second such late-stage trial win for the therapy.  Access the Pipeline Prospector Dashboard for February 2026 Newsmakers (Free Excel)Our viewThe rapidly shifting geopolitical landscape, particularly the conflict in the Middle East and rising trade tensions, is adding a fresh layer of uncertainty for the industry. If the deal-making momentum and progress in clinical trials are maintained, we can safely assume that the innovation pipeline is resilient, the geopolitical turbulence notwithstanding. 

Impressions: 1577

https://www.pharmacompass.com/pipeline-prospector-blog/pipeline-prospector-february-2026-highlights-gilead-buys-arcellx-for-us-7-8-bn-fda-okays-vanda-s-psychotic-pill

#PharmaFlow by PHARMACOMPASS
05 Mar 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: 961

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://firstwordpharma.com/story/7534337

FIRSTWORD PHARMA
07 Jun 2026

https://www.globenewswire.com/news-release/2026/05/05/3287485/0/en/dupixent-dupilumab-demonstrates-improved-esophageal-function-in-eosinophilic-esophagitis-eoe-phase-4-trial.html

GLOBENEWSWIRE
05 May 2026

https://www.fiercepharma.com/pharma/sanofi-expects-extend-its-loe-dupixent-beyond-2031

FIERCE PHARMA
24 Apr 2026

https://www.fiercepharma.com/pharma/sanofi-expects-extend-its-loe-dupixent-beyond-2031

FIERCE PHARMA
23 Apr 2026

https://www.biospace.com/business/sanofi-defends-dupixent-patents-but-execs-insist-it-has-nothing-to-do-with-ceo-change

BIOSPACE
23 Apr 2026

https://www.sanofi.com/en/media-room/press-releases/2026/2026-04-22-21-30-00-3279472

PRESS RELEASE
22 Apr 2026