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Hoth Therapeutics Receives Protocol Approval For HT-001 Cancer Therapeutic; FDA Approved Trial Now Has Two Sites Approved With Additional Sites In Approval Process

By Happy Mohamed
July 19, 8:05 AM
FDA Approved Trial Now Has Two Sites Approved with Additional Sites in Approval Process Recruitment of Patients to Accelerate NEW YORK, July 19, 2023 /PRNewswire/ -- Hoth Therapeutics, Inc. (NASDAQ:HOTH), a

HOTH

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  • Cannabis
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Compatibility Of Psilocybin & SSRIs For Depression, COMPASS Looks At ‘Psychedelic-Assisted Therapies’

By Lara Goldstein
July 18, 3:54 PM
COMPASS Pathways (NASDAQ: CMPS) shared results from an open-label Phase 2 trial assessing its synthetic psilocybin COMP360 alongside SSRIs for Treatment-Resistant Depression (TRD.)

CMPS

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Medtronic Recall Certain Heart Failure Devices Citing Risk Of Low, No Energy Output During High Voltage Therapy

By Vandana Singh
July 18, 12:44 PM
Medtronic Plc (NYSE: MDT) has 

MDT

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Why Are Karyopharm Therapeutics Shares Gaining Today?

By Vandana Singh
July 18, 9:12 AM
Karyopharm Therapeutics Inc (NASDAQ: KPTI) shares are trading higher after the FDA granted Fast Track Designation to the development program of selinexor for myelofibrosis, including primary myelofibrosis, post-essential thrombocythemia myelofibrosis, and post-

KPTI

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AstraZeneca-Sanofi’s Respiratory Syncytial Virus Treatment Scores FDA Approval To Prevent Infection In Infants

By Vandana Singh
July 18, 9:07 AM
The FDA approved AstraZeneca Plc (NASDAQ:

AZN

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What’s Going On With Meta Stock Monday?

By Anusuya Lahiri
July 17, 11:32 AM
Meta Platforms, Inc (NASDAQ: META) stock is trading lower Monday amid reports of possible penalty from Norway regulator for 

META

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‘Quidel Cardiovascular Inc. Recalls Quidel Triage Cardiac Panels For Risk Of False Negative Troponin Results That Could Cause Delayed Diagnosis Or Missed Myocardial Infarction’

By Happy Mohamed
July 17, 9:06 AM
https://www.fda.gov/medical-devices/medical-device-recalls/quidel-cardiovascular-inc-recalls-quidel-triage-cardiac-panels-risk-false-negative-troponin-results   The FDA has identified this as a Class I recall, the

QDEL

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FDA Approves Gilead’s Remdesivir For COVID-19 Treatment Patients With Severe Renal Impairment

By Vandana Singh
July 14, 11:23 AM
The FDA approved Gilead Sciences Inc's (NASDAQ: GILD) supplemental new drug application for using Veklury (remdesivir) in COVID-19 patients with severe renal impairment, 

GILD

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Nutriband Increases Existing Credit Line To $5M Supporting The Continued Development Of Its AVERSA Platform Towards FDA Submission

By Happy Mohamed
July 14, 9:21 AM
https://nutriband.com/news/nutriband-increases-existing-credit-line-to-5-million-usd-supporting-the-continued-development-of-its-aversa-platform-towards-fda-submission Company targeting FDA submission in the first half

NTRB

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CEL-SCI Concludes Meeting With U.S. FDA Concerning Multikine’s Approval For Head & Neck Cancer

By Happy Mohamed
July 14, 9:15 AM
FDA acknowledges the great need for improved treatments for head and neck cancer, particularly the locally advanced oral cavity that CEL-SCI is targeting and is open to a close collaboration with CEL-SCI to help

CVM

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