Hoth Therapeutics Announces HT-ALZ Therapeutic Shows Cognitive Improvements In Alzheimer’s Disease Mouse Model; Shares Halted On Circuit Breaker
July 12, 10:26 AM
Hoth Therapeutics, Inc. (NASDAQ:HOTH), a patient-focused biopharmaceutical company, today announced proof-of-concept data generated using cognitive and behavioral assessments in an Alzheimer's disease
Abbott’s Deep Brain Stimulation Receives FDA’s Breakthrough Device Tag To Manage Depression
July 12, 10:20 AM
The FDA has granted Breakthrough Device Designation to Abbott Laboratories (NYSE:ABT) deep brain stimulation (DBS) system in treatment-resistant depression (TRD), a form…
‘Delaware Health Officials Report First Probable Case Of Monkeypox’ -CBS Philly
July 12, 10:17 AM
https://philadelphia.cbslocal.com/2022/07/12/delaware-first-monkeypox-case/
Rhythm Shares Climb Following Positive Interim Results From Mid-Stage Obesity Study
July 12, 9:42 AM
Rhythm Pharmaceuticals (NASDAQ: RYTM) announced positive interim results from a Phase 2 clinical trial evaluating setmelanotide for the treatment of severe obesity and hyperphagia in people living with hypothalamic obesity.
Y-mAbs’ Announces Clearance of IND For GD2-SADA
July 12, 9:15 AM
NEW YORK, July 12, 2022 (GLOBE NEWSWIRE) -- Y-mAbs Therapeutics, Inc. (the "Company" or "Y-mAbs") (NASDAQ:YMAB) a commercial-stage biopharmaceutical company focused on the development and
Abbott Receives FDA’s Breakthrough Device Designation To Explore Use Of Deep Brain Stimulation To Manage Severe Depression
July 12, 9:09 AM
Breakthrough Device Designations are given by the U.S. FDA to expedite the review of technologies that can improve the lives of people with life-threatening or debilitating conditions
Each year, 2.8 million Americans
Synlogic Initiates Phase 1 Study of SYNB1353 for the Treatment of Homocystinuria
July 12, 7:08 AM
Expected data in H2 2022 brings Synlogic to three clinical readouts this year
Third candidate in less than two years to enter the clinic; Reflects productivity of Synthetic Biotic platform
CAMBRIDGE, Mass., July
Verve Therapeutics Doses First Human With An Investigational In Vivo Base Editing Medicine, VERVE-101, As A Potential Treatment For Heterozygous Familial Hypercholesterolemia
July 12, 6:32 AM
Phase 1b Clinical Trial, heart-1, Now Underway and Enrolling Patients with Heterozygous Familial Hypercholesterolemia in New Zealand
Company Executing VERVE-101 Global Regulatory Strategy with Potential