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Biotech

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  • FDA
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CDC Says Will No Longer Require Air Passengers Traveling To U.S. To Show Negative Covid-19 Viral Test Or Documentation Of Recovery From Covid-19 Before Boarding Flight

By Benzinga Newsdesk
July 12, 12:14 PM
-Reuters

AZN

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  • FDA
  • Movers
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Hoth Therapeutics Announces HT-ALZ Therapeutic Shows Cognitive Improvements In Alzheimer’s Disease Mouse Model; Shares Halted On Circuit Breaker

By Benzinga Newsdesk
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

HOTH

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  • FDA
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Abbott’s Deep Brain Stimulation Receives FDA’s Breakthrough Device Tag To Manage Depression

By Vandana Singh
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…

ABT

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  • FDA
  • News

‘Delaware Health Officials Report First Probable Case Of Monkeypox’ -CBS Philly

By Benzinga Newsdesk
July 12, 10:17 AM
https://philadelphia.cbslocal.com/2022/07/12/delaware-first-monkeypox-case/

AEMD

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  • Biotech
  • General
  • Health Care
  • Penny Stocks

Rhythm Shares Climb Following Positive Interim Results From Mid-Stage Obesity Study

By Ragothaman Srinivasan
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.

RYTM

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  • Biotech
  • General

Y-mAbs’ Announces Clearance of IND For GD2-SADA

By Bill Haddad
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

YMAB

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3 minute read
  • Biotech
  • FDA
  • General
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Abbott Receives FDA’s Breakthrough Device Designation To Explore Use Of Deep Brain Stimulation To Manage Severe Depression

By Bill Haddad
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

ABT

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2 minute read
  • Biotech
  • General

Synlogic Initiates Phase 1 Study of SYNB1353 for the Treatment of Homocystinuria

By Bill Haddad
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

SYBX

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3 minute read
  • Biotech
  • General

Verve Therapeutics Doses First Human With An Investigational In Vivo Base Editing Medicine, VERVE-101, As A Potential Treatment For Heterozygous Familial Hypercholesterolemia

By Bill Haddad
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

VERV

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  • FDA
  • News

UPDATE: Greenwich LifeSciences Says FDA Is Currently Reviewing Manufacturing Data, Has Sent Co. Follow Up Questions To Which Co. Has Responded; Co. Says 3rd Lot Was Manufactured In Commercial Facility On Automated Filling Line

By Michael Horton
July 11, 5:11 PM
-Reuters

GLSI

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