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DATA COMPILATION #PharmaFlow

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Top Pharma Companies & Drugs in 2024: Merck’s Keytruda maintains top spot as Novo’s semaglutide nips at its heels
In 2024, Big Pharma players consolidated and maintained their dominance, even as innovation continued to reshape the pharmaceutical landscape. The primary change last year was the meteoric rise of glucagon-like peptide-1 (GLP-1) receptor agonists that treat diabetes and help in weight loss.Amongst drugmakers, Pfizer retained its numero uno spot with an impressive US$ 63.6 billion in prescription drug sales (up 7 percent from US$ 59.56 billion reported in 2023), despite ever-shrinking Comirnaty sales, which settled at US$ 5.35 billion in 2024 (from US$ 11.22 billion in 2023).Merck secured the second position with revenues of US$ 57.4 billion, a growth of 7 percent over 2023. This performance was predominantly fueled by Keytruda, which now accounts for more than half of Merck’s total pharmaceutical revenue. Johnson & Johnson came a close third with US$ 57 billion in prescription drug sales (up from US$ 54.76 billion in 2023).AbbVie held the fourth position with US$ 56.33 billion in sales, achieving 3.7 percent growth despite the ongoing erosion of Humira revenue. This flagship immunology drug saw sales plummet 37.6 percent to approximately US$ 9 billion, a US$ 5.4 billion reduction compared to 2023. Humira’s loss was offset by AbbVie’s newer immunology assets, particularly Skyrizi and Rinvoq, both of which demonstrated exceptional growth trajectories. View Our Interactive Dashboard on Top Drugs in 2024 by Sales (Free Excel Available)European giants Astra, Roche, Novartis, Sanofi round out top 10 list; Novo, Lilly see astounding growthWhile the top four positions were dominated by American drugmakers, European giants dominated the lower half of the top 10 list.AstraZeneca secured the fifth spot with US$ 54.1 billion in sales, thereby posting impressive growth of 18.1 percent over 2023. Roche claimed the sixth position with US$ 50.9 billion in sales while Novartis ranked seventh — with sales of US$ 50.3 billion. Novartis' impressive 10.8 percent sales growth is attributed to its innovative medicines portfolio. Oncology therapies remained a cornerstone for both these Swiss drugmakers.Bristol Myers Squibb (BMS) secured eighth position with revenues of US$ 48.3 billion, representing 7.3 percent growth over the previous year. At US$ 45 billion, Eli Lilly posted 32 percent revenue growth last year. Its GLP-1 drug Mounjaro helped Lilly move up from the tenth in 2023 to the ninth spot last year.Sanofi landed the tenth position with US$ 42.6 billion in sales, propelled largely by the expanding indications of Dupixent. The French multinational has increasingly focused on this immunology blockbuster, while also garnering more sales from its vaccine and rare disease portfolios.Novo Nordisk merits a mention as it posted an incredible 26 percent year-on-year growth. It retained its eleventh spot with US$ 40.25 billion in sales. Novo’s growth was driven almost exclusively by the extraordinary success of its GLP-1 receptor agonist portfolio. View Our Interactive Dashboard on Top Drugs in 2024 by Sales (Free Excel Available)       Merck’s Keytruda retains throne with US$ 29.5 bn in sales, as Novo’s semaglutide nips at its heelsMoving on to drugs, Merck’s Keytruda (pembrolizumab) solidified its position as the world’s top-selling pharmaceutical product with sales exceeding US$ 29.5 billion and year-on-year growth of 17.88 percent (US$ 4.5 billion). This remarkable performance was driven by steady sales growth across more than 40 indications in the US. In 2024 alone, Keytruda secured four new approvals from the US Food and Drug Administration (FDA).However, Novo Nordisk’s semaglutide sales (Ozempic, Wegovy and Rybelsus) gave Keytruda a run for its money. Across the three blockbuster drugs, semaglutide earned the Danish drugmaker around US$ 28 billion — i.e. a year-on-year increase of 38 percent.Novo’s Ozempic (semaglutide) reached over US$ 16.7 billion in sales — a 20 percent increase from 2023. Originally approved in 2017 to improve glycemic control, Ozempic bagged additional approvals in 2020, and in January 2025. It is now approved to reduce the risk of major cardiovascular events, as well as to reduce cardiovascular risk and to lower the likelihood of chronic kidney disease in type 2 diabetes patients.Sales of Wegovy (semaglutide), the other blockbuster GLP-1 drug from Novo, grew by a whopping 85.7 percent to over US$ 8 billion.Sanofi and Regeneron’s Dupixent (dupilumab) secured the number three spot with sales of US$ 13.6 billion, representing an impressive 17.2 percent year-on-year growth. In 2024, Dupixent received three new approvals and one label update. Notably, it became the first-ever biologic medicine approved for patients with chronic obstructive pulmonary disease (COPD). View Our Interactive Dashboard on Top Drugs in 2024 by Sales (Free Excel Available) AbbVie’s post-Humira strategy pays off as Skyrizi surges 51%; Lilly’s Mounjaro posts 124% growthGilead Sciences’ HIV treatment Biktarvy (bictegravir/emtricitabine/tenofovir alafenamide) showed robust growth of 13.27 percent, touching sales of US$ 13.42 billion in 2024 and emerging as the fourth largest selling drug. Biktarvy now commands over 50 percent of the US HIV treatment market. Unlike many other drugs on this list, Biktarvy faces no immediate patent challenges, with key protections expected to remain intact until 2033.BMS and Pfizer’s anticoagulant Eliquis (apixaban) claimed the fifth position with US$ 13.33 billion in sales, representing a 9.21 percent year-on-year increase. AbbVie’s Skyrizi (risankizumab) emerged as one of the fastest-growing assets with a 50.95 percent year-on-year increase, generating US$ 11.71 billion in 2024 sales, thereby surpassing Humira’s (adalimumab) diminished sales.This impressive performance, combined with Rinvoq’s (upadacitinib) growth, has prompted  AbbVie to raise its long-term outlook for these products. The company now expects combined Skyrizi and Rinvoq revenues to exceed US$ 31 billion by 2027, with Skyrizi alone projected to generate over US$ 20 billion.Johnson & Johnson’s Darzalex (daratumumab) claimed the seventh position with US$ 11.67 billion in sales, representing 19.77 percent growth over 2023.Lilly’s Mounjaro (tirzepatide) demonstrated dramatic growth with sales increasing 123.51 percent to US$ 11.54 billion. This performance was complemented by Zepbound (tirzepatide, for weight loss), which contributed US$ 4.9 billion to Lilly’s revenue. By the end of 2024, Mounjaro received FDA approval for a new indication in obstructive sleep apnea (OSA), becoming the first and only prescription medicine for moderate-to-severe OSA in adults with obesity.Stelara (ustekinumab) ranked ninth, bringing J&J sales of US$ 10.36 billion, showing a modest decline of 4.91 percent from its 2023 sales.Vertex’s triple-combination therapy Trikafta (elexacaftor/tezacaftor/ivacaftor) for treating cystic fibrosis rounded out the top ten list with sales of US$ 10.2 billion, up 14 percent from the previous year. View Our Interactive Dashboard on Top Drugs in 2024 by Sales (Free Excel Available) Our viewIn 2024, transformative therapies like GLP-1 receptor agonists drove growth in the pharmaceutical industry. This year, we expect GLP-1 drugs to dethrone Keytruda from the number one spot. Along with novel immunology agents, we expect GLP-1 drugs to realign the pharmaceutical market.  

Impressions: 15988

https://www.pharmacompass.com/radio-compass-blog/top-pharma-companies-drugs-in-2024-merck-s-keytruda-maintains-top-spot-as-novo-s-semaglutide-nips-at-its-heels

#PharmaFlow by PHARMACOMPASS
24 Apr 2025

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: 1550

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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FDA seeks more safety data from Lilly on obesity drug Foundayo; Novo partners OpenAI to speed up drug development
This week’s Phispers brings you news on how artificial intelligence (AI) is taking centerstage in the world of pharmaceuticals. Novo Nordisk has partnered with OpenAI to deploy AI across its business — from drug discovery to manufacturing and commercial operations. Amazon Web Services launched a new AI-driven platform — Amazon Bio Discovery — to speed up early-stage research. And Novartis CEO Vasant Narasimhan joined the board of AI giant Anthropic.Recently, the US Food and Drug Administration (FDA) had approved Eli Lilly’s GLP-1 obesity drug Foundayo (orforglipron). But this week, there is news that the agency has asked for more data to assess its safety profile, especially risks related to liver injury and cardiovascular events.Johnson & Johnson posted sales of US$ 24.1 billion in the first quarter (Q1), a growth of 9.9 percent. The company has increased its 2026 guidance with estimated sales of US$ 100.8 billion.Meanwhile, FDA has expanded the approval of Travere Therapeutics’ Filspari (sparsentan) to treat a rare kidney disease. The agency declined to approve Replimune’s Tudriqev (vusolimogene oderparepvec) for a second time as a treatment for advanced skin cancer.In news from clinical trials, Eli Lilly’s Jaypirca (pirtobrutinib) showed benefit in chronic lymphocytic leukemia (CLL). And Revolution’s Medicines’ experimental oral drug daraxonrasib ‌helped patients with a highly aggressive form of pancreatic cancer live nearly twice as long as those treated with chemotherapy.An investigation by an Indian newspaper found that counterfeit versions of Merck’s blockbuster Keytruda (pembrolizumab) were being sold to desperate patients in India.In deals, Japan’s Suntory Holdings is acquiring Daiichi Sankyo’s over-the-counter (OTC) drug unit for US$ 1.55 billion. And Australia’s Telix Pharmaceuticals has entered into a collaboration with Regeneron Pharmaceuticals to jointly develop and commercialize next-generation radiopharmaceutical therapies.FDA seeks safety data on Lilly’s newly approved obesity drug FoundayoFDA has asked for more safety data on liver injury linked to Eli Lilly’s Foundayo (orforglipron), a once-daily oral medication approved recently to treat obesity. The approval was fast-tracked under the agency’s new voucher program. FDA has asked Lilly to conduct post-marketing trials to assess risks related to cardiovascular events and stomach emptying. It has also asked the company to conduct a study in lactating women who have received Foundayo to assess concentrations of the drug in breast milk and to obtain more information about the medicine’s potential link to major adverse cardiovascular events and drug-induced liver injury.J&J posts 9.9% sales growth in Q1: Johnson & Johnson is off to a good start in 2026 — it posted sales growth of 9.9 percent to US$ 24.1 billion in Q1 2026, thereby beating analyst expectations. The company has increased its 2026 guidance with estimated reported sales of US$ 100.8 billion.Novo partners OpenAI to speed up drug development; Amazon launches AI platformNovo Nordisk is partnering OpenAI to deploy AI across its business, from drug discovery to manufacturing and commercial operations. The partnership will apply advanced AI capabilities to analyze complex datasets, identify promising drug candidates, and reduce the time required to move a drug from research to patients.Amazon joins the AI-for-drug-discovery race: Amazon Web Services has launched Amazon Bio Discovery, an AI-driven platform designed to speed up early-stage drug discovery by allowing researchers to run complex computational workflows ‌without writing code. These models generate and evaluate potential drug molecules, helping scientists accelerate the development of therapies during the early stages of drug discovery.Meanwhile, AI giant Anthropic has appointed Novartis CEO Vasant Narasimhan to its board of directors.FDA expands approval for Travere’s Filspari to treat rare kidney diseaseFDA has expanded the approval of Travere Therapeutics’ Filspari (sparsentan) to treat a rare kidney disease known as focal segmental glomerulosclerosis  (FSGS) without nephrotic syndrome. In this disease, parts of the filtering units of the kidney are scarred, leading to protein in the urine, swelling and even kidney failure. Filspari is the first and only medicine approved by the FDA for this condition. The drug was originally approved in 2023 for the treatment of IgA nephropathy, another kidney disease.Rejects Replimune’s skin cancer drug:  FDA has declined to approve Replimune’s Tudriqev (vusolimogene oderparepvec) for a second time, after rejecting it last year. Tudriqev was being tested in combination with Bristol Myers Squibb’s Opdivo (nivolumab) to treat an advanced skin cancer. In its complete response letter, the agency has raised concerns about the drug’s reliance on a single‑arm study and has asked Replimune to provide data from a well‑controlled trial.Revolution’s pancreatic cancer drug doubles survival time in key late-stage trialRevolution Medicines’ experimental oral drug — daraxonrasib ‌— helped patients with a highly aggressive form of pancreatic cancer live nearly twice as long as those treated with chemotherapy in a key late-stage trial. The late-stage trial enrolled patients with metastatic pancreatic ductal adenocarcinoma (PDAC) for whom previous treatment had failed. In an interim analysis of a late-stage trial, daraxonrasib achieved overall survival of 13.2 months compared to 6.7 months for chemotherapy.Lilly’s Jaypirca shows benefit in lymphocytic leukemia: Eli Lilly’s Jaypirca (pirtobrutinib) scored a phase 3 win in chronic lymphocytic leukemia (CLL), a slow-growing cancer of the blood and bone marrow. The study showed that adding Jaypirca to a fixed-duration regimen of venetoclax and rituximab significantly extended progression-free survival (PFS), compared with the standard combination alone. Treatment in both study arms was administered for up to two years.Counterfeit Keytruda case exposes oncology supply-chain gaps in IndiaAn investigation by The Indian Express has revealed that counterfeit versions of Merck’s blockbuster immunotherapy Keytruda (pembrolizumab) were allegedly sold to desperate patients in India after genuine vials were diverted from top hospitals in the country. The report also points out how Merck “deployed tactics to inflate the volume of prescriptions and keep the price high through lobbying, while seeking to prevent cheaper versions of Keytruda from reaching hundreds of thousands of cancer patients”.Japan’s Suntory Holdings to buy Daiichi Sankyo’s OTC drug unit for US$ 1.55 billionJapanese beverage group Suntory Holdings will acquire the over-the-counter(OTC) drug unit of Daiichi Sankyo for 246.5 billion yen (US$ 1.55 billion). The stock transfer is scheduled to be completed by June 2029. Meanwhile, Merck and Daiichi Sankyo have been granted FDA’s priority review of their biologics license application for ifinatamab deruxtecan to treat extensive-stage small cell lung cancer (ES-SCLC)Regeneron partners Australia’s Telix: Australia’s Telix Pharmaceuticals has entered into a collaboration with Regeneron Pharmaceuticals to jointly develop and commercialize next-generation radiopharmaceutical therapies. The collaboration will include multiple solid tumor targets from Regeneron’s portfolio of antibodies.

Impressions: 2330

https://www.pharmacompass.com/radio-compass-phisper/fda-seeks-more-safety-data-from-lilly-on-obesity-drug-foundayo-novo-partners-openai-to-speed-up-drug-development

#Phispers by PHARMACOMPASS
16 Apr 2026

NEWS #PharmaBuzz

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https://www.prnewswire.com/news-releases/abbvie-presents-new-data-across-its-blood-cancer-portfolio-at-eha-2026-302793180.html

PR NEWSWIRE
08 Jun 2026

https://www.globenewswire.com/news-release/2026/06/02/3305195/35186/en/kura-oncology-and-kyowa-kirin-announce-publication-in-blood-of-ziftomenib-plus-venetoclax-azacitidine-combination-in-patients-with-r-r-npm1-m-aml.html

GLOBENEWSWIRE
02 Jun 2026

https://www.prnewswire.com/news-releases/lilly-to-spotlight-growing-hematology-portfolio-at-2026-european-hematology-association-eha-annual-meeting-302787526.html

PR NEWSWIRE
02 Jun 2026

https://www.prnewswire.com/news-releases/abbvie-announces-european-commission-authorization-of-expanded-label-for-venclyxto-venetoclax-to-include-additional-combinations-in-previously-untreated-chronic-lymphocytic-leukemia-302785157.html

PR NEWSWIRE
29 May 2026

https://www.prnewswire.com/news-releases/phase-ii-data-from-a-randomized-double-blind-trial-of-ligufalimab-anti-cd47-combination-therapy-in-frontline-aml-published-at-eha-2026-302773386.html

PR NEWSWIRE
15 May 2026

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=214733

FDA
15 May 2026