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Systematic, data-driven science coverage · Monday, October 12, 2026
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Tempest secures option on Senlang’s clinical-stage lentiviral in vivo CAR-T platform
Business

Tempest secures option on Senlang’s clinical-stage lentiviral in vivo CAR-T platform

California-based Tempest Therapeutics (Nasdaq: TPST) has secured an exclusive option to license China-based Hebei Senlang Biotechnology's CD7-targeted...

4d ago
Japan approves Viatris’ Wakix for narcolepsy and OSAS-related daytime sleepiness
Regulatory & Policy

Japan approves Viatris’ Wakix for narcolepsy and OSAS-related daytime sleepiness

Japan's Ministry of Health, Labour and Welfare has approved Wakix (pitolisant) for two indications: excessive daytime sleepiness (EDS) associated with...

4d ago
Elvinix picks up Zealand's GLP-1/gastrin portfolio for type 1 diabetes development
Business

Elvinix picks up Zealand's GLP-1/gastrin portfolio for type 1 diabetes development

Delaware-based Elvinix Inc. has secured an exclusive worldwide license from Zealand Pharma A/S (Nasdaq Copenhagen: ZEAL) to develop and commercialize...

4d ago
IASO Bio’s CD20-targeted in vivo CAR-T cleared for US study in B-NHL
Regulatory & Policy

IASO Bio’s CD20-targeted in vivo CAR-T cleared for US study in B-NHL

China-based IASO Biotechnology received US FDA IND clearance for IASO208, an in vivo CD20-targeted CAR-T therapy for relapsed/refractory B-cell non-Hodgkin...

4d ago
WHO review highlights SynAct’s resomelagon among six dengue drugs for further development
Development

WHO review highlights SynAct’s resomelagon among six dengue drugs for further development

A World Health Organization review of the dengue therapeutic pipeline has identified resomelagon as one of six candidates with sufficient supporting...

4d ago
ReEmerge exits stealth with USD 37m Series A to advance TBI brain stimulation study
Business

ReEmerge exits stealth with USD 37m Series A to advance TBI brain stimulation study

Minnesota-based ReEmerge, Inc. has launched from stealth with an oversubscribed USD 37 million Series A financing to advance an implantable deep brain...

4d ago
Novartis exercises option to acquire Sironax blood-brain barrier delivery platform for USD 125m
Business

Novartis exercises option to acquire Sironax blood-brain barrier delivery platform for USD 125m

Novartis (NYSE: NVS) has exercised its exclusive option to acquire Sironax's proprietary Brain Delivery Module (BDM) platform, completing a transaction...

4d ago
Sensorion targets US IPO with SEC filing as it pivots to GJB2 gene therapy
Business

Sensorion targets US IPO with SEC filing as it pivots to GJB2 gene therapy

France-based hearing loss biotech Sensorion (Euronext: ALSEN) has confidentially submitted a draft registration statement on Form F-1 to the US Securities...

4d ago
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Sling starts Phase III trial of oral TED therapeutic linsitinib
Development

Sling starts Phase III trial of oral TED therapeutic linsitinib

Michigan-based Sling Therapeutics has dosed the first patients in the ORBIT pivotal trial, a global Phase III study of linsitinib in moderate to severe...

4d ago
Twist joins Lilly's TuneLab as preferred antibody characterization data provider
Business

Twist joins Lilly's TuneLab as preferred antibody characterization data provider

South San Francisco-based Twist Bioscience Corporation (Nasdaq: TWST) has joined Lilly TuneLab, Eli Lilly's collaborative AI/ML drug discovery platform, as...

4d ago
Pfizer follows AstraZeneca in pulling EU bladder cancer filing after CHMP concerns
Regulatory & Policy

Pfizer follows AstraZeneca in pulling EU bladder cancer filing after CHMP concerns

Pfizer's European marketing authorization application for Zumrad (sasanlimab), a subcutaneous anti-PD-1 monoclonal antibody intended for use with Bacillus...

4d ago
China grants breakthrough status to CSPC’s EGFR ADC in AGA-negative NSCLC
Regulatory & Policy

China grants breakthrough status to CSPC’s EGFR ADC in AGA-negative NSCLC

CSPC Pharmaceutical Group Ltd (HKEX: 01093) announced that China's National Medical Products Administration (NMPA) has granted Breakthrough Therapy...

4d ago
Takeda secures FDA Priority Review for oral TYK2 inhibitor zasocitinib
Regulatory & Policy

Takeda secures FDA Priority Review for oral TYK2 inhibitor zasocitinib

The US FDA has accepted for Priority Review a New Drug Application (NDA) from Takeda (NYSE: TAK) for zasocitinib (TAK-279), an oral tyrosine kinase 2 (TYK2)...

4d ago
Shennon raises USD 12m to advance three preclinical T-cell engagers
Business

Shennon raises USD 12m to advance three preclinical T-cell engagers

San Francisco-based Shennon Biotechnologies has raised USD 12 million in a new financing round and simultaneously disclosed three oncology programs built on...

4d ago
Orvida secures Recordati-led financing for ontivatrep in rare genetic skin diseases
Business

Orvida secures Recordati-led financing for ontivatrep in rare genetic skin diseases

Israel-based Orvida Pharma Ltd, formerly Kamari Pharma, a clinical-stage biotechnology company developing treatments for rare and severe genetic skin...

4d ago