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Electra Therapeutics Announces $183 Million Series C Financing to Advance First-in-Class SIRP-Targeted Therapies for Immune Disorders and Cancer

October 22, 2025
Proceeds will fund a global pivotal trial of lead product candidate, ELA026, as a frontline treatment for secondary hemophagocytic lymphohistiocytosis...
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Electra Logo

Electra Therapeutics Announces $183 Million Series C Financing to Advance First-in-Class SIRP-Targeted Therapies for Immune Disorders and Cancer

October 22, 2025
Proceeds will fund a global pivotal trial of lead product candidate,...
Read More
Portfolio News
Electra Logo

Electra Therapeutics Announces First Patients Dosed in the SURPASS Phase 2/3 Pivotal Study of ELA026 in Secondary Hemophagocytic Lymphohistiocytosis (sHLH)

October 22, 2025
The SURPASS study is enrolling patients at research sites across the...
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Electra Therapeutics Receives FDA Breakthrough Therapy and EMA Priority Medicines Designations for ELA026 in Secondary Hemophagocytic Lymphohistiocytosis (sHLH)

October 22, 2025
ELA026 has demonstrated promising potential as a frontline treatment for patients...
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AllRock Bio Presents Phase 1 Data for Lead Program, ROC-101, at the ERS Congress

September 29, 2025
ROC-101 exhibits favorable pharmacokinetics for once-daily dosing
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All Rock Bio logo

AllRock Bio Announces $50 Million Series A to Advance Lead Clinical Program for Pulmonary Hypertension

September 16, 2025
Funding to advance first-in-class pan-ROCK inhibitor through Phase 2a testing in...
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Portfolio News

Checking in on the progress of CAR-T for autoimmune conditions with the CEO of Kyverna – the company’s first (and first for the field) registration intended trial will read in the first half of 2026

August 13, 2025
Warner Biddle describes the trajectory of the field, and how neuro-autoimmune...
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Portfolio News

Neuron23 Announces $96.5 Million Series D Financing and First Patient Dosed in Global Phase 2 NEULARK Clinical Trial of NEU-411 for Early Parkinson’s Disease

June 24, 2025
NEULARK trial to evaluate NEU-411, a brain-penetrant, potent and selective LRRK2...
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Capsida Receives FDA IND Clearance for Its IV-Administered Gene Therapy for Parkinson’s Disease Associated with GBA Mutations

June 11, 2025
Capsida is initiating the Phase 1/2 study for CAP-003, with the...
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Portfolio News

Capsida Presents New GLP Toxicology Data Supporting Recent FDA IND Clearance of Its First-in-Class, IV-administered Gene Therapy for STXBP1 Developmental and Epileptic Encephalopathy

May 14, 2025
Capsida Presents New GLP Toxicology Data Supporting Recent FDA IND Clearance...
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