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Sunday, 15 November 2026
EVIDENCE. INTERPRETED.
Pharmacally

Disease & Drugs

Approvals, trial readouts, research and drug safety alerts, interpreted by pharmacists and checked against the primary source.

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Latest in Disease & Drugs

1,785 stories · every one Fact-Checked
Vasa Therapeutics VS-041 oral MMP inhibitor targeting cardiac fibrosis and fibroinflammation in heart failure with preserved ejection fraction.Clinical TrialsVasa Reports NT-proBNP Reduction With VS-041 in HFpEF TrialVasa Therapeutics reports positive Phase 1c results for VS-041, with reduced NT-proBNP after 28 days in patients with HFpEF.12 Nov 2026 · 4 min read
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Beeline Medicines' investigational TLR7/8 inhibitor afimetoran demonstrates positive Phase 2 results in systemic lupus erythematosus.Clinical TrialsBeeline Reports Positive Phase 2 Results for Afimetoran in SLEBeeline Medicines reported positive Phase 2 results for afimetoran in systemic lupus erythematosus, with all three doses meeting the primary endpoint.12 Nov 2026 · 4 min read
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Regeneron’s CIDEBsiRNA RNA interference therapy targeting liver fat reduction in MASLD.Clinical TrialsRegeneron’s CIDEB siRNA Sustains 80% Liver Fat ReductionRegeneron’s investigational CIDEBsiRNA reduced liver fat by up to 80% through week 36 following a single dose in adults with MASLD.12 Nov 2026 · 4 min read
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Amgen's dazodalibep demonstrates Phase 3 improvements in systemic disease activity and patient-reported dryness in Sjögren's disease.Clinical TrialsAmgen’s Dazodalibep Meets Phase 3 Goal in Sjögren’s DiseaseAmgen’s dazodalibep met the primary endpoint in the Phase 3 OASIZ-301 trial, with both dosing regimens reducing systemic disease activity at Week 48.12 Nov 2026 · 5 min read
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Abbisko's pimicotinib (PIMJETMI) CSF-1R inhibitor receives FDA approval for symptomatic tenosynovial giant cell tumor (TGCT).New Drug ApprovalAbbisko’s PIMJETMI Wins FDA Approval After 56% Response in TGCTAbbisko Therapeutics’ pimicotinib (PIMJETMI), an oral CSF-1R inhibitor, has received FDA approval for adults with symptomatic tenosynovial giant cell tumor (TGCT).12 Nov 2026 · 4 min read
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Novartis investigational anti-BAFF-R antibody ianalumab shows sustained reduction in Sjögren’s disease activity in the NEPTUNUS extension study.Clinical TrialsNovartis Reports Two-Year Ianalumab Results in Sjögren’s DiseaseNovartis presented Week 108 findings from the NEPTUNUS extension study, showing further reductions in systemic disease activity with monthly ianalumab in patients with Sjögren’s disease.12 Nov 2026 · 4 min read
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Beam Therapeutics risto-cel base-editing therapy achieves primary efficacy endpoint in the BEACON trial for severe sickle cell disease.Clinical TrialsBeam Reports Positive BEACON Results for Risto-cel in SCDBeam Therapeutics’ investigational base-editing therapy risto-cel met the primary efficacy endpoint and all secondary efficacy endpoints in the BEACON Phase 1/2 trial, demonstrating 12-month freedom from severe vaso-occlusive…12 Nov 2026 · 4 min read
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FDA class-wide NAION safety warning for GLP-1 receptor agonists following analysis of 126 randomized clinical trials.Drugs Safety AlertFDA Requires Class-Wide NAION Warning for GLP-1 DrugsThe FDA is requiring class-wide NAION labeling updates for GLP-1 receptor agonists after reviewing 126 randomized trials involving 134,253 patients.10 Nov 2026 · 4 min read
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Bayer SUNHARBO (asundexian) receives FDA approval as the first Factor XIa inhibitor for secondary stroke prevention.New Drug ApprovalBayer’s SUNHARBO Wins FDA Approval as First Factor XIa InhibitorBayer secures FDA approval for SUNHARBO (asundexian) 50 mg, the first Factor XIa inhibitor for secondary stroke prevention.10 Nov 2026 · 3 min read
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Alnylam AMVUTTRA vutrisiran five-year HELIOS-B study findings in transthyretin amyloidosis with cardiomyopathyClinical TrialsAlnylam Highlights 5-Year Cardiovascular Benefits of VutrisiranAlnylam’s five-year HELIOS-B findings demonstrate sustained cardiovascular benefits with early and continuous vutrisiran treatment in patients with ATTR-CM, including lower mortality and recurrent cardiovascular event risks, better-preserved quality…10 Nov 2026 · 5 min read
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Merck efinopegdutide Phase 2b trial showing MASH resolution and liver fibrosis improvement in adults with F2–F3 MASH.Clinical TrialsMerck Reports Positive Phase 2b Results for Efinopegdutide in MASHMerck’s investigational GLP-1/glucagon receptor co-agonist efinopegdutide achieved its primary endpoint in a Phase 2b MASH trial, with 63% resolution at the 7 mg dose versus 13% with placebo.…10 Nov 2026 · 4 min read
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Boehringer Ingelheim's investigational dual GLP-1 and glucagon receptor agonist survodutide meets the cardiovascular safety endpoint in the Phase III SYNCHRONIZE-CVOT trial.Clinical TrialsBoehringer Reports Positive Phase III CV Safety Results for SurvodutideBoehringer Ingelheim’s survodutide met the primary cardiovascular safety endpoint in the Phase III SYNCHRONIZE-CVOT trial involving 5,530 adults with overweight or obesity and elevated cardiovascular risk.9 Nov 2026 · 4 min read
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