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Systematic, data-driven science coverage · Monday, September 14, 2026
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AbbVie's atogepant meets primary endpoint in Phase III menstrual migraine trial
Development

AbbVie's atogepant meets primary endpoint in Phase III menstrual migraine trial

Atogepant (Qulipta/Aquipta) met the primary endpoint and all eight ranked secondary endpoints in the Phase III LUNA trial evaluating preventive treatment of...

4d ago
ViaNautis expands into spinal cord injury with SCI Ventures backing for polyNaut platform
Business

ViaNautis expands into spinal cord injury with SCI Ventures backing for polyNaut platform

Cambridge, UK-based ViaNautis Bio has secured investment from SCI Ventures to expand its non-viral genetic medicine delivery platform into chronic spinal...

4d ago
NodThera rebrands as Rezera as ruvonoflast meets Phase II endpoint, eyes Phase III in PAD
Development

NodThera rebrands as Rezera as ruvonoflast meets Phase II endpoint, eyes Phase III in PAD

Ruvonoflast (NT-0796), an oral NLRP3 inflammasome inhibitor developed by Boston-based Rezera Inc. (formerly NodThera), met its primary endpoint in the...

4d ago
Mindera Health partners with UPenn to investigate quinacrine mechanism in lupus
Business

Mindera Health partners with UPenn to investigate quinacrine mechanism in lupus

Mindera Health is collaborating with University of Pennsylvania researchers to investigate why quinacrine helps some patients with cutaneous lupus—and...

4d ago
Seismic launches global Phase III trial of istaroxime in cardiogenic shock
Development

Seismic launches global Phase III trial of istaroxime in cardiogenic shock

Durham, North Carolina-based Seismic Pharmaceuticals has launched a global Phase III trial of istaroxime in cardiogenic shock, a life-threatening condition...

4d ago
UpDoc receives up to USD 9.2m from ARPA-H for autonomous heart failure AI system
Business

UpDoc receives up to USD 9.2m from ARPA-H for autonomous heart failure AI system

Palo Alto-based UpDoc has been selected as a lead performer in the Advanced Research Projects Agency for Health (ARPA-H) ADVOCATE program, receiving an...

4d ago
Cytonics crowdfunds USD 4.8m to advance A2M biologic into Phase Ib/IIa osteoarthritis study
Business

Cytonics crowdfunds USD 4.8m to advance A2M biologic into Phase Ib/IIa osteoarthritis study

Jupiter, Florida-based Cytonics Corporation has completed a USD 4.8 million gross-proceeds financing campaign, bringing total capital raised to USD 47...

4d ago
Insightec spinout Lotus Neuro launches brain drug delivery platform
Business

Insightec spinout Lotus Neuro launches brain drug delivery platform

Lotus Neuro, a clinical-stage biotechnology company spun out of focused ultrasound specialist Insightec, launched publicly with a platform designed to...

4d ago
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Disc Medicine’s DISC-3405 reduces phlebotomy needs in Phase II polycythemia vera trial
Development

Disc Medicine’s DISC-3405 reduces phlebotomy needs in Phase II polycythemia vera trial

Massachusetts-based Disc Medicine (Nasdaq: IRON) released Phase II data showing that DISC-3405, an anti-TMPRSS6 monoclonal antibody, sharply reduced...

4d ago
Insilico’s rentosertib becomes first AI-discovered drug to enter Phase III
Development

Insilico’s rentosertib becomes first AI-discovered drug to enter Phase III

Insilico Medicine (HKEX: 3696) has dosed the first patient in GENESIS-IPF-3, the Phase III trial of rentosertib (ISM001-055 / INS018\055) in idiopathic...

4d ago
Tempus wins USD 9.5m in ARPA-H funding to develop autonomous cardiology AI
Business

Tempus wins USD 9.5m in ARPA-H funding to develop autonomous cardiology AI

Tempus AI (Nasdaq: TEM) secured up to USD 9.5 million from the Advanced Research Projects Agency for Health (ARPA-H) to develop and clinically validate an...

4d ago
Roche moves Enspryng toward first approved MOGAD therapy
Regulatory & Policy

Roche moves Enspryng toward first approved MOGAD therapy

Roche (SIX: RO; OTCQX: RHHBY) announced a US FDA Priority Review award for a supplemental Biologics License Application (sBLA) for Enspryng (satralizumab),...

4d ago
Bayer’s Hyrnuo joins Boehringer’s Hernexeos in first-line HER2-mutant NSCLC
Regulatory & Policy

Bayer’s Hyrnuo joins Boehringer’s Hernexeos in first-line HER2-mutant NSCLC

The US FDA has granted accelerated approval to Hyrnuo (sevabertinib) for the first-line treatment of adults with locally advanced or metastatic non-squamous...

4d ago
McGill and Mount Sinai researchers identify PRMT7 as suppressor of CD8+ T cell expansion
Discovery

McGill and Mount Sinai researchers identify PRMT7 as suppressor of CD8+ T cell expansion

A protein arginine methyltransferase acts as a previously unrecognized suppressor of cytotoxic T cell proliferation, offering a potential new target for...

4d ago
BioNTech ends autogene cevumeran Phase II after OS imbalance favors control
Development

BioNTech ends autogene cevumeran Phase II after OS imbalance favors control

The BNT122-01 Phase II trial of autogene cevumeran in resected colorectal cancer has been terminated after an independent data safety monitoring board...

4d ago