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DATA COMPILATION #PharmaFlow

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J&J’s Intra‑Cellular buyout, BMS’ oncology gambit, Sanofi’s Blueprint acquisition drive mega deals in H1 2025
The pharmaceutical industry has witnessed a wave of mergers, acquisitions, and strategic partnerships so far in the first half (H1) of 2025, with deal values exceeding US$ 170 billion.PharmaCompass’ data shows oncology alone accounted for nearly US$ 47 billion in deal value, followed by US$ 18 billion each in immunology and psychiatry, US$ 17 billion in nutrition/weight loss and US$ 7 billion in neurology.Pharma majors such as Johnson & Johnson and Bristol Myers Squibb led with two deals worth over US$ 10 billion each. Sanofi executed a series of deals in the immunology and neuro-inflammation space. And Eli Lilly stood out for its aggressive dealmaking, which spanned oncology, pain, RNA therapies, and AI-driven oligonucleotides. In all, it signed seven deals worth over US$ 1 billion each. View Pharma & Biotech Acquisitions, Deals & Agreements in 2025 as of June 14 (Free Excel Available)H1 records several mega deals as J&J buys Intra-Cellular, BMS ties up with BioNTech, Sanofi acquires BlueprintJohnson & Johnson dominated headlines with its US$ 14.6 billion acquisition of Intra-Cellular Therapies in January 2025. This marks the largest biopharma deal since Novo Nordisk’s US$ 16.5 billion acquisition of Catalent in February 2024. This acquisition positions J&J as a formidable player in the neuroscience space. Bristol Myers Squibb entered into a US$ 11.1 billion partnership with BioNTech. The deal structure — US$ 3.5 billion in unconditional payments and up to US$ 7.6 billion in milestone payments — demonstrates BMS’ confidence in BNT327, a next-generation bispecific antibody in phase 3 trials for treating extensive stage small cell lung cancer and non-small cell lung cancer.Sanofi acquired Blueprint Medicines for US$ 9.5 billion in order to enhance its rare disease portfolio. The French drugmaker is also creating a comprehensive immunology portfolio. The company signed a US$ 1.9 billion deal for Dren Bio’s DR-0201 bispecific antibody for autoimmune diseases. Sanofi also acquired Vigil Neuroscience for US$ 470 million for its phase 2-ready Alzheimer’s disease candidate. Additionally, the drugmaker secured a US$ 1.84 billion global license agreement with Earendil Labs for two next-generation bispecific antibodies.Pfizer’s US$ 6.05 billion partnership with 3SBio provides it global licensing rights (excluding China) for SSGJ-707, a bispecific antibody currently undergoing multiple clinical trials in China for non-small cell lung cancer, metastatic colorectal cancer, and gynecological tumors. View Pharma & Biotech Acquisitions, Deals & Agreements in 2025 as of June 14 (Free Excel Available) Obesity gold rush sees Roche, AbbVie, Sciwind ink deals; Novo pledges over US$ 5 bn across three dealsThe obesity therapeutics market has triggered intense competition among pharmaceutical giants. Roche’s US$ 5.3 billion partnership with Zealand Pharma is focused on petrelintide, an amylin analog designed to preserve lean mass better than existing GLP-1-based treatments. The collaboration combines petrelintide with Roche’s dual GLP-1/GIP receptor agonist CT-388, creating a differentiated obesity treatment.Market leader Novo Nordisk has promised over US$ 5 billion across three major obesity deals in 2025. The US$ 2.2 billion Septerna collaboration targets oral small molecule medicines for obesity and cardiometabolic diseases.Novo signed a separate US$ 2 billion agreement with China’s United Biotechnology for UBT251, a triple agonist for GLP-1, GIP, and glucagon receptors in phase 2 clinical development for obesity, type 2 diabetes, and other diseases. The company’s third major deal, a US$ 1 billion partnership with Lexicon Pharmaceuticals, provides it access to LX9851, a molecule in preclinical development for obesity and associated metabolic disorders.Sciwind Biosciences secured a US$ 2.5 billion global licensing and collaboration agreement with Verdiva Bio Limited for the global development and commercialization of a portfolio of metabolic diseases therapies. AbbVie entered the amylin arena through its US$ 2.2 billion Gubra partnership for GUB014295, a candidate in phase 1 trials for treating obesity. View Pharma & Biotech Acquisitions, Deals & Agreements in 2025 as of June 14 (Free Excel Available) Molecular glue degraders draw investments; Lilly signs seven deals over US$ 1 billion eachMolecular glue degraders have emerged as a transformative therapeutic modality, attracting significant investment across multiple partnerships. AbbVie’s US$ 1.64 billion collaboration with Neomorph leverages the biotech’s leading molecular glue discovery platform for oncology and immunology applications.Genentech’s potential US$ 2.1 billion partnership with Orionis Biosciences focuses on small-molecule monovalent glue medicines for novel and challenging oncology targets. This is the second partnership between the two companies, following their initial 2023 collaboration.Eli Lilly has collaborated with Magnet Biomedicine, utilizing Magnet’s TrueGlue discovery platform for oncology applications. The deal could be worth up to US$ 1.3 billion.Eli Lilly has emerged as one of 2025’s most active dealmakers, with approximately seven deals exceeding US$ 1 billion each. The company’s US$ 2.5 billion Scorpion Therapeutics acquisition provides access to STX-478, an experimental oral therapy in early-stage trials for breast cancer and advanced solid tumors, potentially addressing 30 to 40 percent of hormone-positive breast cancer patients.On June 17, Lilly announced the acquisition of gene-editing startup Verve Therapeutics for US$ 1.3 billion. Lilly’s US$ 1 billion SiteOne acquisition announced in May brings STC-004, a phase 2-ready non-opioid chronic pain treatment to its pipeline. Other partnerships announced by Lilly include a US$ 1.4 billion capsid licensing deal with Sangamo for central nervous system disease genomic medicines and a US$ 1.3 billion collaboration with South Korean company Rznomics for RNA-based hearing loss treatments. Lilly has also strengthened its oligonucleotide pipeline through a potential US$ 1 billion collaboration with Creyon Bio for AI-designed oligonucleotide therapies targeting RNA. View Pharma & Biotech Acquisitions, Deals & Agreements in 2025 as of June 14 (Free Excel Available) Merck KGaA acquires SpringWorks for US$ 3.9 bn; Novartis buys out Anthos for US$ 3.1 bnAstraZeneca signed a US$ 5.3 billion AI-led research agreement with China’s CSPC Pharmaceuticals Group to advance the discovery of novel oral candidates for immunological diseases. Merck KGaA acquired SpringWorks for US$ 3.9 billion in April, which gave it access to two FDA-approved therapies — Ogsiveo (nirogacestat), the first and only approved therapy for adult patients with progressing desmoid tumors requiring systemic treatment, and Gomekli (mirdametinib), the first and only FDA-approved therapy for adults and children with neurofibromatosis type 1-associated plexiform neurofibromas.Novartis’ US$ 3.1 billion Anthos Therapeutics acquisition centered around abelacimab, a potential first-in-class monoclonal antibody currently in three phase 3 studies for stroke and systemic embolism prevention in atrial fibrillation patients.GSK’s US$ 2 billion acquisition of Boston Pharmaceuticals’ efimosfermin targets steatotic liver disease (fatty liver disease). The medicine is also in clinical development for MASH treatment. GSK’s second major deal involved the US$ 1.15 billion acquisition of US biotech IDRx, strengthening its gastrointestinal cancer portfolio.The pharma industry also drew some private equity interest as Bain Capital acquired Japan’s Mitsubishi Tanabe Pharma from Mitsubishi Chemical Group for US$ 3.3 billion. View Pharma & Biotech Acquisitions, Deals & Agreements in 2025 as of June 14 (Free Excel Available) Our viewDespite an uncertain geopolitical environment, the year has seen a surge in M&As and dealmaking in the first half of 2025. However, a sizable chunk of the acquisitions were bolt-on transactions, indicating that companies are not ready to take on risks, and are buying out smaller players who strategically fit into their operations. Going forward, there are indications that M&A activity will stay strong throughout 2025. 

Impressions: 6705

https://www.pharmacompass.com/radio-compass-blog/j-j-s-intra-cellular-buyout-bms-oncology-gambit-sanofi-s-blueprint-acquisition-drive-mega-deals-in-h1-2025

#PharmaFlow by PHARMACOMPASS
19 Jun 2025

STOCK RECAP #PipelineProspector

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Pipeline Prospector March 2025: Trump’s FDA overhaul spooks biotech stocks; Roche, AbbVie, Novo ink obesity drug deals
March ended with news that the top vaccine regulator of the US Food and Drug Administration (FDA), Peter Marks, was forced to resign. This impacted pharma indices adversely. The Nasdaq Biotechnology Index (NBI) dropped 6.22 percent from 4,525.73 in February to 4,244.37 in March. The SPDR S&P Biotech ETF (XBI) fell 8.61 percent from 88.74 to 81.10, and the S&P Biotechnology Select Industry Index (SPSIBI) declined 8.61 percent from 6,914.8 to 6,319.5. The sector has been under pressure ever since US President Donald Trump announced plans to impose potential 25 percent tariffs on pharmaceutical imports. Just last week, Johnson & Johnson committed US$ 55 billion to set up four new manufacturing plants in the US. J&J’s announcement follows Eli Lilly’s US$ 27 billion US investment pledge announced in February. Merck too is deepening its domestic footprint with the inauguration of a new US$ 1 billion, 225,000-square-foot vaccine manufacturing facility in Durham, North Carolina, as part of its broader US $20 billion US investment strategy spanning 2018 to 2028.Trump’s trade policy is also driving corporate decisions. In an opportunistic maneuver, Mallinckrodt and Endo — both emerging from bankruptcy due to opioid litigation — decided to merge via a US$ 6.7 billion deal that strategically leverages their extensive US manufacturing capabilities. The new company will focus on branded drugs, and hopes to benefit from tariffs on imported goods.  Access the Pipeline Prospector Dashboard for March 2025 Newsmakers (Free Excel)  Roche, AbbVie ink US$ 5.3 bn, US$ 2.2 bn deals for amylin-based obesity treatments; AstraZeneca strikes multiple dealsMarch saw competition in the obesity treatment market intensify with multiple pharmaceutical giants making strategic moves. The month witnessed a rise in interest in amylin-based treatments. Amylin is a peptide hormone that plays a role in regulating blood sugar and appetite. The amylin pathway has the potential advantage of reducing fat rather than lean muscle.Roche signed a US$ 5.3 billion agreement with Zealand Pharma for petrelintide, a promising long-acting amylin analog administered weekly through a subcutaneous injection. Zealand will receive an upfront payment of US$ 1.65 billion from Roche. AbbVie marked its entry into the lucrative obesity market through an up to US$ 2.23 billion licensing agreement with Danish biotech firm Gubra for GUB014295, another amylin-targeting drug.Towards the end of the month, Novo Nordisk announced a US$ 1 billion licensing deal with Lexicon Pharmaceuticals for the latter’s experimental obesity drug. Under the terms of the deal, Novo will get worldwide rights to develop, manufacture and commercialize the drug, LX9851, for obesity and associated metabolic disorders.Novo also secured ex-China rights to United Laboratories International Holdings’ UBT251 in a deal worth up to US$ 2 billion. This is a "triple-G" drug that targets three receptors — GLP-1, GIP, and glucagon — involved in regulating blood sugar and appetite.Similarly, Merck entered into a US$ 2 billion-worth agreement with Jiangsu Hengrui Pharmaceuticals for HRS-5346, an oral drug targeting lipoprotein(a) reduction to prevent cardiovascular diseases.In immunology, Sanofi’s US$ 1.9 billion acquisition of Dren Bio’s immunology unit centered around DR-0201, a novel treatment for autoimmune diseases that targets specific immune cells (B-cells) that mistakenly attack healthy cells. Early clinical studies suggest this approach could potentially reset the adaptive immune system, offering sustained remission for patients with refractory conditions like lupus.AstraZeneca has been particularly active this month. Astra announced a US$ 1 billion acquisition of Belgian cell therapy biotech EsoBiotec and a US$ 1.35 billion agreement with Alteogen to develop subcutaneous formulations of its oncology drugs. The acquisition brings AstraZeneca the innovative ENaBL platform, which could transform cell therapy by reducing treatment times from weeks to minutes while significantly lowering manufacturing costs.The British-Swedish drugmaker also announced collaborations with Chinese biotech firms, Harbour BioMed and Syneron Bio, as well as a joint venture with BioKangtai to develop, produce, and market vaccines for respiratory and other infectious diseases.Oncology-focused biopharma Chimerix got acquired by Jazz Pharmaceuticals for US$ 935 million. Its lead candidate dordaviprone is currently under FDA review for treating H3 K27M-mutant diffuse glioma, a rare brain tumor.  Access the Pipeline Prospector Dashboard for March 2025 Newsmakers (Free Excel)  GSK’s Blujepa, Roche’s TNKase mark first breakthroughs in 30 years for uUTI, acute ischemic stroke treatmentsThe month saw two key FDA approvals — GSK’s Blujepa and Roche’s TNKase. GSK’s Blujepa (gepotidacin) is the first new class of oral antibiotics for uncomplicated urinary tract infections (uUTIs) in nearly three decades. The drug, approved for the treatment of uUTIs in female adults and patients aged 12 years and older who weigh at least 40 kg, has a novel mechanism of action that offers hope against certain antibiotic-resistant strains.Similarly, the US approval of Roche’s TNKase (tenecteplase) for acute ischemic stroke marks the first new treatment option for stroke patients in nearly 30 years. Its five-second administration offers a critical advantage in time-sensitive stroke management.Sanofi and Alnylam’s RNAi therapy Qfitlia (fitusiran) became the first approved treatment for both hemophilia A and B. And Novartis’ prostate cancer drug Pluvicto won an expanded approval to treat PSMA-positive metastatic castration-resistant prostate cancer (mCRPC) before taxane-based chemotherapy.Alnylam Pharmaceuticals (stock up 9 percent in March) secured FDA approval for Amvuttra (vutrisiran) to treat cardiomyopathy of wild-type or hereditary ATTR-CM, making it the first medication approved in the US to address both ATTR-CM and polyneuropathy of hereditary transthyretin-mediated amyloidosis.  Access the Pipeline Prospector Dashboard for March 2025 Newsmakers (Free Excel)  Novo’s CagriSema underwhelms in late-stage trial; J&J’s med fails, serving another blow to depression treatment March also saw several high-profile clinical disappointments. Novo Nordisk’s (stock down 23 percent) CagriSema (cagrilintide/semaglutide) delivered underwhelming results in its second late-stage obesity trial. While the drug demonstrated superior weight loss compared to Wegovy, showing 13.7 percent average weight reduction over 68 weeks, market expectations for a breakthrough superior to rival Eli Lilly’s Mounjaro (tirzepatide) were not met.The neurology segment continued to see disappointments, especially in the treatment of depression. J&J’s aticaprant failed in late-stage depression studies for major depressive disorder (MDD), forcing the company to abandon its development for this indication. The disappointing results come on the heels of similar setbacks within the same drug class, most notably with Neumora Therapeutics’ navacaprant.  Access the Pipeline Prospector Dashboard for March 2025 Newsmakers (Free Excel)  Our viewThe pharmaceutical landscape has been undergoing dramatic changes since Trump moved into the White House for a second term. The most significant change for the sector is FDA’s overhaul. For decades, FDA has been the gold standard for drug regulation. The overhaul has changed that.“The FDA as we’ve known it is finished,” former FDA Commissioner Robert Califf said in a social media post. Healthcare investment bankers are already talking about large deals getting stalled as executives grapple with the volatile policy scenario. Given these uncertainties, our sentiments are bearish, at least for the short term.  Access the Pipeline Prospector Dashboard for March 2025 Newsmakers (Free Excel)  

Impressions: 4453

https://www.pharmacompass.com/pipeline-prospector-blog/pipeline-prospector-march-2025-trump-s-fda-overhaul-spooks-biotech-stocks-roche-abbvie-novo-ink-obesity-drug-deals

#PharmaFlow by PHARMACOMPASS
03 Apr 2025

NEWS #PharmaBuzz

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https://www.fiercebiotech.com/biotech/novo-nordisk-hails-remarkable-weight-loss-oral-glp-1-drug

FIERCE BIOTECH
11 Sep 2024