News
BellaSeno Establishes High-Profile Clinical Advisory Board
— Leading international experts to support clinical development of BellaSeno´s pioneering resorbable breast implants
— Pivotal clinical trial to be initiated shortly
BellaSeno GmbH, an ISO 13485-certified medtech company developing resorbable scaffolds using additive manufacturing technologies, today announced that the Company has established a Clinical Advisory Board consisting of seven renowned key opinion leaders (KOLs) in the fields of clinical breast reconstruction and plastic surgery. Read more…
Mabylon AG Raises CHF 30 Million to Advance Peanut Allergy Lead Program MY006 to Clinical Proof-of-Concept
— Funding combines equity investment and convertible loan
— Focus on best-in-class, clinical-stage peanut allergen neutralizing antibody
— Further potential for developing Mabylon’s discovery and pre-clinical pipeline programs
— Thomas Hecht has joined Board of Directors
Mabylon AG, a leader in the high-throughput discovery, characterization, and development of human-derived antibodies, today announced that it has raised a total of CHF 30 million (USD 37 million) to further develop its clinical-stage lead candidate MY006 and advance its early-stage pipeline. The funding combines a capital increase and a convertible loan of CHF 15 million, respectively. The funds are provided by Mabylon’s existing private investors, with the major investment coming from former management and board members of Roche. Read more…
MetrioPharm’s MP1032 Receives EMA Orphan Drug Designation in Duchenne Muscular Dystrophy
- European Medicines Agency recognizes potential of lead compound MP1032 in addressing a high unmet medical need in Duchenne Muscular Dystrophy (DMD)
- Designation is paving the way for safer long-term therapy
- MP1032 has demonstrated ability to preserve muscle function and reduce inflammation without disrupting normal cellular processes
Zurich, July 29, 2025 – MetrioPharm AG, a pharmaceutical company developing drugs for inflammatory and infectious diseases, announced today that the European Medicines Agency has granted Orphan Drug Designation (ODD) to its lead compound, MP1032 for the treatment of children affected by Duchenne muscular dystrophy (DMD). Read more…
Ebenbuild Secures Euro 2.3 Million EIC Grant to Scale Digital Twin Platform for Respiratory Health
— Funding supports market launch of platform for clinical and commercial applications
— Company targets Euro 15 billion in silico trials market and ICU decision support
Ebenbuild, a company developing personalized, AI-enabled digital twins of lungs to support clinical decisions and digital clinical trials, today announced that it has received Euro 2.3 million funding under the European Innovation Council (EIC) Accelerator program to advance its digital twin platform technology. In addition, the EIC fund will invest up to €10 million in future equity financing rounds raised by Ebenbuild. Read more…