AllSci News

Systematic, data-driven science coverage · Tuesday, August 4, 2026
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Development

Soligenix’s HyBryte shows improved response and tolerability vs Valchlor in small CTCL study

Soligenix (Nasdaq: SNGX) reported that a small comparative study of synthetic hypericin (HyBryte) versus mechlorethamine (Valchlor) in cutaneous T-cell...

Apr 2
Business

Inovio raises USD 17.5m in underwritten public offering

INOVIO Pharmaceuticals, Inc. (Nasdaq: INO) announced a USD 17.5 million underwritten public offering on April 2, 2026, seeking to extend its cash runway as...

Apr 2
Development

Oric's PRC2 inhibitor rinzimetostat combo regimen advances to Phase III trial in mCRPC

ORIC Pharmaceuticals (Nasdaq: ORIC) reported Phase Ib dose optimization data for rinzimetostat in combination with darolutamide in post-abiraterone...

Apr 2
Development

Novo Nordisk follows Lilly's oral GLP-1 approval with data showing Wegovy's weight loss advantage

Novo Nordisk (NVO) reported that oral semaglutide 25 mg (Wegovy) produced approximately 3 percentage points more weight loss than orforglipron in a...

Apr 2
News

Fore Bio’s plixorafenib receives FDA Breakthrough Therapy status for BRAF-mutated glioma

Fore Biotherapeutics, a registration-stage oncology company headquartered in Philadelphia, Pennsylvania, announced that the FDA has granted Breakthrough Therapy Designation (BTD) to plixorafenib…

Apr 2
Development

Alto discontinues transdermal PDE4 inhibitor after Phase II failure in schizophrenia-linked cognitive impairment

Alto Neuroscience (NYSE: ANRO) reported that ALTO-101 failed to meet its primary EEG or cognitive endpoints versus placebo in a Phase II proof-of-concept...

Apr 2
Business

Shionogi acquires global RADICAVA rights from Tanabe Pharma for USD 2.5b

Shionogi Acquires Global RADICAVA Rights for USD 2.5 Billion from Tanabe Pharma Corporation

Apr 2
News

A2’s logic-gated, IL-12-tethered CAR-T takes FDA Fast Track for MSLN solid tumors

A2 Biotherapeutics, headquartered in Agoura Hills, California, announced receipt of US FDA Fast Track Designation for A2B543, an autologous logic-gated chimeric antigen…

Apr 2
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Business

Gilead Sciences extends deadline for Arcellx tender offer

Gilead Sciences Consolidates Full Ownership of Multiple Myeloma CAR T Programme via USD 120.00 Per Share Acquisition of Arcellx

Apr 2
News

Alpha Cognition receives USPTO patent for ALPHA-1062 traumatic brain injury treatment method

Vancouver-based Alpha Cognition Inc., (NASDAQ: ACOG), a biopharmaceutical company focused on neurodegenerative disorder therapy, received US Patent No. 12,589,099 from the USPTO,…

Apr 2
News

FDA approves Eli Lilly’s oral GLP-1 Foundayo for weight loss

The US FDA approved Eli Lilly and Company’s oral GLP-1 receptor agonist orforglipron (Foundayo) on April 1, 2026 for chronic weight management…

Apr 1
News

Zai Lab and Amgen collaborate on DLL3-targeting dual mechanism strategy for SCLC

Zai Lab (NASDAQ: ZLAB; HKEX: 9688) and Amgen (NASDAQ: AMGN) have entered a global clinical trial collaboration and supply agreement to evaluate…

Apr 1
News

Ray Therapeutics’ RTx-015 optogenetic gene therapy earns RMAT designation for retinitis pigmentosa

Ray Therapeutics, a clinical-stage biopharmaceutical company headquartered in Berkeley, California, has announced that the FDA has granted Regenerative Medicine Advanced Therapy (RMAT)…

Apr 1
Regulatory & Policy

FDA extends review of Orca Bio's Orca-T for hematologic malignancies to July 2026

Orca Bio has announced that the US FDA extended the review timeline for its Biologics License Application (BLA) for Orca-T, an investigational allogeneic...

Apr 1
Business

Nuvation Bio takes global control of IDH1 drug safusidenib through Japan market deal with Daiichi Sankyo

Safusidenib, an oral brain-penetrant inhibitor of mutant IDH1, will now advance under a single global rights holder after Nuvation Bio (NYSE: NUVB) amended...

Apr 1