AllSci News

Systematic, data-driven science coverage · Saturday, August 1, 2026
Latest News
Idorsia secures USD 278m debt facility to extend runway as insomnia franchise scales
Business

Idorsia secures USD 278m debt facility to extend runway as insomnia franchise scales

Switzerland-based Idorsia Pharmaceuticals Ltd (SWX: IDIA) confirmed the closing of a senior secured term loan facility of up to CHF 250 million...

Jun 26
Ligand raises USD 700m to fund USD 739m XOMA royalty acquisition
Business

Ligand raises USD 700m to fund USD 739m XOMA royalty acquisition

Jupiter, Florida-based Ligand Pharmaceuticals Incorporated (Nasdaq: LGND) announced the closing of a USD 700 million offering of 0.00% convertible senior...

Jun 26
News

Boehringer Ingelheim taps Immunai’s AI to map T-cell targets across cancer and autoimmune disease

Boehringer Ingelheim and New York-based Immunai announced a multi-project discovery collaboration valued at up to USD 15 million, extending through 2027, focused…

Jun 26
Arcus enters immunology with first-in-human MRGPRX2 antagonist for atopic disease
Development

Arcus enters immunology with first-in-human MRGPRX2 antagonist for atopic disease

Arcus Biosciences (NYSE: RCUS) has registered a first-in-human trial of AB102, an oral small-molecule antagonist of MRGPRX2 (Mas-related G-protein-coupled...

Jun 26
Nuvation Bio raises USD 250m in convertible notes
Business

Nuvation Bio raises USD 250m in convertible notes

New York-based Nuvation Bio, Inc. (NYSE: NUVB) announced the pricing of an upsized convertible senior notes offering totaling USD 250 million, with proceeds...

Jun 26
Arrowhead launches mysterious RNAi candidate ARO-033 with undisclosed target and mechanism
Development

Arrowhead launches mysterious RNAi candidate ARO-033 with undisclosed target and mechanism

Arrowhead Pharmaceuticals (Nasdaq: ARWR) has registered a first-in-human trial for ARO-033, an investigational subcutaneous agent that appears to be derived...

Jun 26
MaaT Pharma challenges EMA rejection of Xervyteg with re-examination request for aGvHD
Regulatory & Policy

MaaT Pharma challenges EMA rejection of Xervyteg with re-examination request for aGvHD

France-based MaaT Pharma (Euronext: MAAT) has announced its intention to request a re-examination of the negative opinion issued by the European Medicines...

Jun 26
Discovery

HSS researchers uncover hidden driver of rheumatoid arthritis beyond inflammation

Researchers at the Hospital for Special Surgery (HSS) Research Institute in New York have identified a distinct immune cell population that appears to drive...

Jun 26
The AllSci BriefSystematic R&D and deal news. Daily.
Optimeos secures backing for non-viral nano gene therapy delivery
Business

Optimeos secures backing for non-viral nano gene therapy delivery

Princeton, New Jersey-based Optimeos Life Sciences has announced an investment from Hatch BioFund, an early-stage life sciences venture capital firm...

Jun 26
Otsuka reports positive Phase IIIb anxiety data as centanafadine nears July FDA decision
Development

Otsuka reports positive Phase IIIb anxiety data as centanafadine nears July FDA decision

Otsuka has reported positive Phase IIIb results for centanafadine sustained-release in adults with ADHD and comorbid anxiety, a readout that matters because...

Jun 25
University of Pennsylvania investigates discontinuing anti-CD20 therapy in relapsing MS
Discovery

University of Pennsylvania investigates discontinuing anti-CD20 therapy in relapsing MS

The University of Pennsylvania has received a USD 1.34 million NIH U01 award to conduct a randomized, placebo-controlled trial testing whether ocrelizumab...

Jun 25
Epitopea's mRNA vaccine targets ovarian cancer's treatment-resistant majority with first-in-human trial
Development

Epitopea's mRNA vaccine targets ovarian cancer's treatment-resistant majority with first-in-human trial

Epitopea's mRNA cancer vaccine CryptiVax-1001 enters first-in-human testing in ovarian cancer's hardest-to-treat subgroup

Jun 25
HUTCHMED's fanregratinib posts pivotal Phase II data as China NDA enters priority review
Development

HUTCHMED's fanregratinib posts pivotal Phase II data as China NDA enters priority review

HUTCHMED's fanregratinib demonstrated a 42.5% objective response rate in pretreated patients with FGFR2 fusion-positive intrahepatic cholangiocarcinoma,...

Jun 25
Mwyngil reports one of the first public in vivo datasets for GPR75 obesity program
Development

Mwyngil reports one of the first public in vivo datasets for GPR75 obesity program

Boston-based Mwyngil Therapeutics reported preclinical proof-of-concept data for its GPR75 inverse agonist obesity program, with lead oral compounds...

Jun 25
Lycia raises USD 75m to advance novel extracellular protein degradation into early clinical trials
Business

Lycia raises USD 75m to advance novel extracellular protein degradation into early clinical trials

South San Francisco-based Lycia Therapeutics, Inc., a clinical-stage biotechnology company developing therapeutics designed to degrade disease-causing...

Jun 25