Palvella Therapeutics Announces Positive Topline Results from Phase 2 Study of QTORIN™ 3.9% Rapamycin Anhydrous Gel (QTORIN™ rapamycin) for the Treatment of Microcystic Lymphatic Malformations, a Serious, Rare Genetic Skin Disease with No FDA-approved Therapies

– QTORIN™ rapamycin generally well-tolerated; no drug related severe adverse events and no observed rapamycin in systemic circulation 

– 100% of participants were either “Much Improved” or “Very Much Improved” as rated by the Clinician Global Impression of Change following 12-weeks of QTORIN™ rapamycin 

– End of Phase 2 meeting completed with U.S. Food and Drug Administration in February 2023; pending additional interactions with FDA, anticipate potential initiation of pivotal Phase 3 study in second half of 2023

– FDA previously granted Fast Track Designation and Orphan Drug Designation to QTORIN™ rapamycin for Microcystic Lymphatic Malformations 

– QTORIN™ rapamycin has potential to become first therapy and standard of care for the estimated more than 30,000 individuals with Microcystic Lymphatic Malformations in U.S., if approved 

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VESTECK, Inc. is pleased to announce the first in human use of several SUTURE-TIGHT devices

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Venatorx Pharmaceuticals Appoints Tomas J. Heyman as Non-Executive Chairman

Dr. Michael Diem Steps Down from Board of Directors

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Hanimune Therapeutics raises $3.3M, sets sights on first food allergy treatment product

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Palvella Therapeutics Announces Pipeline Update on QTORIN™ 3.9% Rapamycin Anhydrous Gel (QTORIN™ Rapamycin) for Serious, Rare Genetic Skin Diseases with No FDA-approved Therapies

– Pivotal Phase 3 data for the treatment of Pachyonychia Congenita anticipated mid-2023 –

– Phase 2 data for the treatment of Microcystic Lymphatic Malformations anticipated March 2023 –

– Phase 2b data for the prevention of Basal Cell Carcinomas in patients with Gorlin Syndrome anticipated 2Q 2023 –

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Immunome Announces Formation of Antibody-Drug Conjugate and T Cell Redirection Advisory Board

Advisory board to help guide selection of novel antibody-target pairs for ADC and T cell redirection modalities

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Annovis Bio Announces Approval for European Union Clinical Trial Sites for the Phase 3 Study of Buntanetap for the Treatment of Parkinson’s Disease

The Company was Granted Approval for an Additional 48 sites Across Five European Union Countries

Annovis Currently has 50 Clinical Trial Sites Open in the United States

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Services for the UnderServed (S:US) Partners with Ride Health to Improve Transportation for Clients with Intellectual and Developmental Disabilities (I/DD)

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Annovis Bio Announces Filing of Patent Covering the Administration of Buntanetap and Its Analogues for the Treatment of Mental Illnesses

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iVIEW Therapeutics announces a successful pre-IND meeting with FDA and Received its Full Agreement on Development Plans for IVW-1001, a Novel Treatment for Dry Eye Disease

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