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STOCK RECAP #PipelineProspector

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Pipeline Prospector Jan 2026 highlights: Astra, CSPC sign up to US$ 18.5 bn obesity deal; Wegovy’s pill version debuts in US
The year 2026 began amid heightened geopolitical tensions, particularly over Greenland. The US President Donald Trump threatened 25 percent tariff on several European countries until the US is allowed to purchase Greenland, a semi-autonomous Danish territory. These threats escalated transatlantic tensions and drew strong pushback from European nations and NATO.Despite this, biotech indices grew steadily through the month. The Nasdaq Biotechnology Index (NBI) rose 2.26 percent in January, moving from 5,723.48 to 5,852.67. The SPDR S&P Biotech ETF (XBI) gained 2.03 percent, climbing from 122.27 to 124.75, while the S&P Biotechnology Select Industry Index (SPSIBI) increased 2.29 percent, rising from 9,528.24 to 9,746.25.The month also saw Big Pharma continuing to pledge investments in the US to avert tariffs. January is also the month of JP Morgan healthcare conference. This year, the meet (or JPM26) saw announcements of several important deals, especially in the sphere of obesity drugs and the use of artificial intelligence in drug discovery. Access the Pipeline Prospector Dashboard for January 2026 Newsmakers (Free Excel)Astra, CSPC sign up to US$ 18.5 bn obesity deal; AbbVie to invest US$ 100 bn in USAstraZeneca made a lot of news last month. It signed an up to US$ 18.5 billion licensing deal with China’s CSPC Pharmaceutical Group for its  experimental obesity and weight-related drug candidates. AstraZeneca will pay US$ 1.2 billion upfront and up to US$ 17.3 billion in milestones. The package includes a clinical-ready and three pre-clinical candidates in CSPC’s injectable weight-management portfolio. AstraZeneca will also collaborate with CSPC on four additional new programs using CSPC’s sustained-release delivery platform and AI-driven peptide drug discovery. Besides this deal, AstraZeneca also announced a US$ 15 billion investment in China through 2030 to expand medicines manufacturing and R&D, including capabilities in cell therapy and radio-conjugates.In the US, pharma companies continued to announce investments to avoid import tariffs threatened by Trump. AbbVie pledged US$ 100 billion into its US research, development and manufacturing operations over the next 10 years. This is, by far, the biggest commitment announced by a drugmaker. Coming in at a distant second is Johnson & Johnson, which had announced US$ 55 billion in US-based investments in March.Similarly, Eli Lilly said it will build a US$ 3.5 billion manufacturing plant in Pennsylvania to produce injectable weight-loss medicines, with construction expected to begin in 2026 and operations planned for 2031.Roche’s Genentech also said it will invest nearly US$ 2 billion in a new bio-manufacturing facility in Holly Springs, North Carolina, to manufacture next-generation metabolic treatments, including obesity medicines. Access the Pipeline Prospector Dashboard for January 2026 Newsmakers (Free Excel) AI deals in Jan: Astra buys Modella AI; Sanofi ties up with Earendil; Lilly-Nimbus in obesity research dealArtificial intelligence is taking centerstage in dealmaking. AstraZeneca agreed to acquire Boston-based Modella AI (deal size not disclosed), integrating its foundation models and AI agents into oncology R&D to support clinical development and biomarker discovery.Similarly, Sanofi signed an AI-powered autoimmune and inflammatory disease collaboration worth up to US$ 2.56 billion with Earendil Labs, which will receive up to US$ 160 million in upfront and near-term payments. Sanofi will lead development and commercialization of bispecific candidates from the partnership.Lilly also signed a multi-year AI-driven obesity research and licensing agreement with Nimbus Therapeutics worth up to US$ 1.3 billion. Additionally, Lilly and Nvidia announced an expanded AI partnership, including a US$ 1 billion co‑innovation lab in the Bay Area (US) to integrate advanced computing and biology for drug discovery. This announcement was made at JPM26. Access the Pipeline Prospector Dashboard for January 2026 Newsmakers (Free Excel)Novo’s Wegovy pill makes blockbuster debut in US; Darzalex Faspro quadruplet wins FDA nodIn January, the pill version of Novo Nordisk’s Wegovy (semaglutide) made a stunning debut in the US. It was prescribed more than 18,000 times in the first full week after ‌its launch. Novo’s stock price went up by 14 percent during the month.Johnson & Johnson secured an approval from the US Food and Drug Administration (FDA) for Darzalex Faspro (daratumumab and hyaluronidase) as part of a four-drug regimen for newly diagnosed multiple myeloma patients ineligible for an autologous stem cell transplant. The combination includes Darzalex Faspro with Velcade (bortezomib), Revlimid (lenalidomide) and dexamethasone. The approval marks Darzalex Faspro’s 12th indication overall and its fifth in the newly diagnosed multiple myeloma setting.Darzalex (daratumumab) remains J&J’s largest growth driver, generating US$ 14.4 billion in 2025 sales. J&J (stock up 10 percent) projected its 2026 revenue to be in the range of about US$ 100 billion to US$ 101 billion.FDA also approved Zycubo (copper histidinate) from Fortress Biotech and Sentynl Therapeutics (a US-based biopharma owned by Zydus Lifesciences), to treat Menkes disease, making it the first FDA-approved therapy for the genetic disorder in the US.On the clinical front, Amgen said its experimental obesity drug MariTide (maridebart cafraglutide) helped patients maintain weight loss when administered at a lower dose or less frequently. Access the Pipeline Prospector Dashboard for January 2026 Newsmakers (Free Excel)AbbVie partners China-based RemeGen in US$ 5.6 bn deal; GSK to acquire RAPT TherapeuticsAbbVie partnered China-based RemeGen in a US$ 5.6 billion oncology deal to develop and commercialize RC148, an experimental therapy for multiple advanced solid tumors. AbbVie will gain rights outside Greater China, while RemeGen will receive US$ 650 million upfront and up to US$ 4.95 billion in milestones, along with double-digit royalties. Britain’s GSK said it will acquire US-based RAPT Therapeutics (stock up 69 percent) in a US$ 2.2 billion deal, gaining global rights to the experimental food allergy drug ozureprubart, excluding rights in mainland China, Macau, Taiwan and Hong Kong.Eli Lilly (stock down 3 percent) entered into a US$ 1.93 billion collaboration with US-based Repertoire Immune Medicines to develop tolerizing therapies (treatments that restore the immune system’s ability to recognize self-antigens) for autoimmune disease targets. Repertoire will receive US$ 85 million upfront and up to US$ 1.84 billion in milestones, while Lilly will take over clinical development and commercialization.Novartis added an Alzheimer’s program to its pipeline through a licensing and collaboration deal with SciNeuro Pharmaceuticals, paying US$ 165 million upfront and up to US$ 1.5 billion in milestones. Access the Pipeline Prospector Dashboard for January 2026 Newsmakers (Free Excel)Our viewThis year, several new medications, including treatments for weight loss, hypertension, smoking cessation and plaque psoriasis, are likely to receive FDA approvals. Moreover, existing medications — such as Dupixent (dupilumab) and Wegovy (semaglutide) — could see expanded indications. January has already set a dynamic tone for the year ahead. 

Impressions: 2621

https://www.pharmacompass.com/pipeline-prospector-blog/pipeline-prospector-jan-2026-highlights-astra-cspc-sign-up-to-us-18-5-bn-obesity-deal-wegovy-s-pill-version-debuts-in-us

#PharmaFlow by PHARMACOMPASS
05 Feb 2026

WEEKLY NEWS RECAP #Phispers

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AbbVie inks US$ 5.6 bn oncology deal with China’s RemeGen; Astra buys Modella AI to speed up cancer drug research
This week’s Phispers is packed with news from the ongoing JP Morgan Healthcare Conference (JPM26). Notably, AbbVie said it is partnering with China-based RemeGen to develop and commercialize an experimental cancer therapy that is designed to treat multiple advanced solid tumors. Novartis entered a worldwide licensing and collaboration deal with SciNeuro Pharmaceuticals to develop a next-generation antibody therapy for Alzheimer’s disease.Artificial intelligence (AI) appeared to be a key focus area at JPM26.  AstraZeneca announced the acquisition of Boston-based AI firm Modella AI, and Nvidia and Eli Lilly expanded their existing collaboration. They have announced a US$ 1 billion five-year investment to set up a joint AI research lab in the San Francisco Bay Area.Meanwhile, Johnson & Johnson and AbbVie struck agreements with the Trump administration to cut drug prices for Americans while expanding US-based manufacturing and R&D investments.The US Food and Drug Administration (FDA) approved Zycubo (copper histidinate), the first US therapy for rare Menkes disease. The agency also asked drugmakers to remove suicidal risk warnings from GLP-1 weight-loss drugs.In news from clinical trials, Eli Lilly said combining Zepbound (tirzepatide) with Taltz (ixekizumab) improved psoriatic arthritis outcomes in a late-stage trial. Bristol Myers Squibb’s Camzyos (mavacamten) met phase 3 goals in adolescents with obstructive hypertrophic cardiomyopathy (oHCM).And, a US judge temporarily blocked the Trump administration from freezing over US$ 10 billion in child welfare funds to five states.J&J, AbbVie strike deals with Trump admin to cut drug prices; AbbVie commits US$ 100 bn in US investmentsAfter the Trump administration signed agreements with 11 large drugmakers in December, Johnson & Johnson and AbbVie have also reached similar agreements.J&J has agreed to lower drug prices for Americans in return for exemptions from US tariffs on its pharmaceutical products. Under the agreement, J&J will participate in the TrumpRx.gov website (yet to be launched). J&J also reaffirmed its US$ 55 billion US investment plan.Similarly, AbbVie entered into a three-year agreement with the Trump administration to reduce prices of select medicines in the US, while committing to invest US$ 100 billion over the next decade in domestic research, development and manufacturing. AbbVie also agreed to expand direct-to-patient sales through the TrumpRx.gov. In return, it will receive tariff exemptions.Meanwhile, AbbVie has agreed to acquire a drug delivery device manufacturing facility and related intellectual property from West Pharmaceutical Services in Tempe, Arizona, as part of its broader push to expand US-based manufacturing.Deals@JPM26: AbbVie inks US$ 5.6 bn oncology deal with China’s RemeGen; Novartis ties up with SciNeuroAbbVie has partnered with China-based RemeGen to develop and commercialize an experimental cancer therapy, RC148, as it looks to strengthen its oncology pipeline. The drug is designed to treat multiple advanced solid tumors, including non-small cell lung cancer and colorectal cancer, where treatment options remain limited. Under the deal, AbbVie will gain rights to develop, manufacture and sell RC148 outside Greater China. RemeGen will receive US$ 650 million upfront and could earn up to US$ 4.95 billion in milestone payments, along with double-digit royalties if the drug reaches the market.Similarly, Novartis has entered a worldwide licensing and collaboration deal with SciNeuro Pharmaceuticals to develop a next-generation antibody therapy for Alzheimer’s disease. SciNeuro will receive US$ 165 million upfront and is eligible for up to US$ 1.5 billion in milestone payments, along with tiered royalties.AI Deals@JPM26: Nvidia, Lilly to invest US$ 1 bn in AI drug research labs; Astra acquires Modella AIAstraZeneca has agreed to acquire Boston-based AI firm Modella AI. This is “the first acquisition of an AI firm by a big pharmaceutical company,” Astra said. Modella’s “foundation models” and AI agents will be integrated into AstraZeneca’s oncology R&D, supporting clinical development, biomarker discovery, and quantitative pathology.Additionally, Nvidia and Eli Lilly have announced a US$ 1 billion five-year investment to set up a joint AI research lab in the San Francisco Bay Area, expanding an existing collaboration between the chipmaker and the drugmaker. The partnership builds on Lilly’s growing use of AI in drug discovery.FDA orders removal of suicidal risk warning from GLP-1 drugs; okays first US drug for Menkes diseaseFDA has asked drugmakers to remove warning about potential suicidal thoughts from GLP-1 weight-loss medications, including Novo Nordisk’s Wegovy (semaglutide) and Saxenda (liraglutide), and Eli Lilly’s Zepbound (tirzepatide). The move follows a review of 91 placebo-controlled clinical trials involving over 107,910 patients, which found no evidence linking GLP-1 receptor agonists to increased risk of suicidal thoughts, behavior, or other psychiatric side effects.Approves Zycubo for rare disease: FDA has approved Zycubo (copper histidinate), a drug developed by Fortress Biotech and Sentynl Therapeutics (a US-based biopharma owned by Zydus Lifesciences), to treat Menkes disease, a rare genetic disorder that prevents children from absorbing copper. This makes Zycubo the first FDA-approved therapy for the condition in the US.Lilly’s Zepbound-Taltz combo improves psoriatic arthritis outcomes in phase 3 trialEli Lilly has said a late-stage study showed that using its weight-loss drug Zepbound (tirzepatide) together with its psoriatic arthritis treatment Taltz (ixekizumab) improved arthritis symptoms and led to greater weight loss than Taltz alone. The trial included overweight or obese adults with psoriatic arthritis, a condition that causes joint pain and is commonly linked to obesity.Amgen’s MariTide helped patients maintain weight loss: Amgen’s experimental obesity drug MariTide (maridebart cafraglutide) helped patients maintain weight loss when given at a lower dose or less frequently, according to a study presented at JPM26. The drug differs from weekly-injection weight-loss treatments, with potential for long-term weight management.BMS’ Camzyos meets phase 3 goals in adolescents with heart disease: Bristol Myers Squibb reported positive topline results from its phase 3 trial of Camzyos (mavacamten) in adolescents aged 12 to under 18 with symptomatic obstructive hypertrophic cardiomyopathy (oHCM). In 2022, Camzyos was granted FDA approval for treating oHCM in adults.US judge blocks Trump admin from freezing US$ 10 bn in child welfare fundsA US federal judge has temporarily blocked the Trump administration from freezing more than US$ 10 billion in childcare and family assistance funds to five Democratic-led states. The restraining order came after California, Colorado, Illinois, Minnesota and New York sued the administration over the funding freeze due to concerns of fraud and misuse of benefits.

Impressions: 1635

https://www.pharmacompass.com/radio-compass-phisper/abbvie-inks-us-5-6-bn-oncology-deal-with-china-s-remegen-astra-buys-modella-ai-to-speed-up-cancer-drug-research

#Phispers by PHARMACOMPASS
15 Jan 2026

NEWS #PharmaBuzz

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https://sentynl.com/news/zycubo-fda-approval/

PRESS RELEASE
12 Jan 2026

https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=211241

FDA
12 Jan 2026

https://www.globenewswire.com/news-release/2025/12/15/3205379/28889/en/Fortress-Biotech-and-Cyprium-Therapeutics-Announce-FDA-Acceptance-of-CUTX-101-NDA-Resubmission.html

GLOBENEWSWIRE
15 Dec 2025