AllSci News

Systematic, data-driven science coverage · Friday, July 31, 2026
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Atea opens first dedicated antiviral program for hepatitis E with AT-587 Phase I trial
Development

Atea opens first dedicated antiviral program for hepatitis E with AT-587 Phase I trial

Atea Pharmaceuticals (Nasdaq: AVIR) has dosed the first participants in a Phase I clinical trial of AT-587, an oral nucleotide analog prodrug, for hepatitis...

Jul 14
ARPA-H awards USD 160m to accelerate rare disease gene editing through umbrella clinical trials
Discovery

ARPA-H awards USD 160m to accelerate rare disease gene editing through umbrella clinical trials

ARPA-H has announced up to USD 160 million in funding over five years for seven performer teams under its THRIVE (Treating Hereditary Rare Diseases with In...

Jul 14
News

FDA accelerates SOTIO’s CDH17-targeting colorectal cancer ADC with Fast Track designation

SOTIO Biotech, a clinical-stage biopharmaceutical company owned by PPF Group and headquartered in Prague with offices in Basel and Boston, announced that…

Jul 14
News

Sino Bio scores first BTD for an AT2R antagonist in China for neuropathic pain

Sino Biopharmaceutical Limited (HKEX: 01177) announced that TRD205, a peripherally-restricted, highly selective angiotensin II type 2 receptor (AT2R) antagonist developed by its…

Jul 14
Spero secures USD 105m non-dilutive financing backed by Utebzi royalties
Business

Spero secures USD 105m non-dilutive financing backed by Utebzi royalties

Cambridge, Massachusetts-based Spero Therapeutics (Nasdaq: SPRO) announced a USD 105 million non-recourse, non-dilutive royalty financing with affiliates of...

Jul 14
HuyaBio's tucidinostat-nivolumab combo cuts melanoma progression risk by 58% in Phase III trial
Development

HuyaBio's tucidinostat-nivolumab combo cuts melanoma progression risk by 58% in Phase III trial

HuyaBio International, which operates out of San Diego and Shanghai, China, has reported statistically significant Phase III results for HBI-8000...

Jul 14
Spero expands into autoimmune disease via USD 1.1b Innovent anti-CD40L deal
Business

Spero expands into autoimmune disease via USD 1.1b Innovent anti-CD40L deal

Spero Therapeutics in-licenses Innovent's Fc-silent anti-CD40L antibody in up to USD 1.1 billion deal, marking a full pivot from antibiotics to autoimmune

Jul 14
AstraZeneca pays USD 600m upfront to reacquire worldwide rights to former China R&D asset from Dizal
Business

AstraZeneca pays USD 600m upfront to reacquire worldwide rights to former China R&D asset from Dizal

AstraZeneca has entered a global exclusive license agreement with China-based Dizal Pharmaceutical (SSE: 688192) for Zegfrovy (sunvozertinib), an oral...

Jul 14
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Hansoh extends cross-border licensing strategy with Avere Nasdaq deal, highlighting evolution of biotech “NewCo” model
Business

Hansoh extends cross-border licensing strategy with Avere Nasdaq deal, highlighting evolution of biotech “NewCo” model

Private US-based Avere Therapeutics, Inc. has entered into a definitive all-stock merger agreement with NextCure, Inc. (Nasdaq: NXTC), a US-based...

Jul 14
News

ADDF and Michael J. Fox Foundation pool USD 5m to develop shared Alzheimer’s-Parkinson’s biomarkers

The Alzheimer’s Drug Discovery Foundation (ADDF) and The Michael J. Fox Foundation for Parkinson’s Research (MJFF) announced a USD 5 million research…

Jul 14
Alto Neuroscience raises USD 100m through stock offering as depression candidate enters Phase III
Business

Alto Neuroscience raises USD 100m through stock offering as depression candidate enters Phase III

Mountain View, California-based Alto Neuroscience, Inc. (NYSE: ANRO) announced the pricing of an underwritten registered direct offering of common stock,...

Jul 14
News

US FDA approves Leqembi Iqlik for at-home subcutaneous initiation in early Alzheimer’s disease

The US FDA approved a supplemental Biologics License Application for Leqembi Iqlik (lecanemab-irmb) subcutaneous injection as an initiation dose for early Alzheimer’s…

Jul 14
BMS seeking first FDA approval for molecular glue mezigdomide in heavily pretreated multiple myeloma
Regulatory & Policy

BMS seeking first FDA approval for molecular glue mezigdomide in heavily pretreated multiple myeloma

The US FDA has accepted for review a New Drug Application submitted by Bristol Myers Squibb (NYSE: BMY) for mezigdomide in combination with carfilzomib and...

Jul 14
News

Novartis signs up to access Chai Discovery’s AI antibody platform

San Francisco-based Chai Discovery announced a collaboration with Novartis under which the Swiss pharmaceutical company will gain access to Chai’s generative AI…

Jul 14
Voyager reports durable six-month preclin safety data for Alzheimer's gene therapy ahead of Phase I
Development

Voyager reports durable six-month preclin safety data for Alzheimer's gene therapy ahead of Phase I

Voyager Therapeutics (Nasdaq: VYGR) reported six-month preclinical toxicology data for VY1706 Alzheimer's gene therapy candidate at the Alzheimer's...

Jul 14