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Atriva Therapeutics Announces Exclusive Letter Agreement for Reverse Takeover Transaction with Biocure Technology

by Paul Lelieveld | Sep 18, 2023 | Meneldor News

Atriva Therapeutics and Canadian Biocure Technologies, Inc. entered into an exclusive letter agreement for a reverse takeover transaction. Upon successful completion of the transaction, the resulting entity will continue the business of Atriva Therapeutics....

Tagworks Pharmaceuticals Announces $65 Million in Series A Financing to Advance Click-to-Release Therapeutics

by Paul Lelieveld | Jun 24, 2023 | Meneldor News

Financing round led by Ysios Capital and Gilde Healthcare with participation from Novartis Venture Fund, New Enterprise Associates, and Lightstone Ventures Unique Click-to-Release platform enables on-target activation of antibody-drug conjugates (ADCs) and...

Atriva Therapeutics appoints Christian Pangratz as Chief Executive Officer, implementing planned management change

by Paul Lelieveld | Nov 9, 2022 | Meneldor News

• Christian Pangratz to become Chief Executive Officer of Atriva Therapeutics GmbH effective January 15, 2023 • Dr. Rainer Lichtenberger, co-founder and CEO, retires after a transition period as Co-CEO of at least six months • With positive POC data from RESPIRE study...

Hemispherian Secures EUR 10M in Financing from the European Innovation Council (EIC) Accelerator Program

by Paul Lelieveld | Oct 19, 2022 | Meneldor News

Oslo, Norway – October 19, 2022 – Hemispherian AS (“Hemispherian” or the “Company”), a Norwegian preclinical pharmaceutical company focused on small molecule cancer therapeutics targeting the DNA damage response, is delighted to announce a successful...

Atriva Therapeutics announces Topline Results from the Proof of Concept (POC) / Phase 2a RESPIRE study (zapnometinib) in patients hospitalized with COVID-19

by Paul Lelieveld | Sep 20, 2022 | Meneldor News

Atriva Therapeutics GmbH announces high-level results from the Phase 2a RESPIRE study Results indicate a clinically relevant efficacy profile for zapnometinib, in terms of the primary endpoint, clinical severity status (CSS) at Day 15, with a favorable safety profile...
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