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UPDATE: Clovis Oncology Says FDA Maintains Their Recommendation That Co. Wait For More Mature Overall Survival Data To Submit SNDA

By Michael Horton
July 6, 4:37 PM
-Reuters

CLVS

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UPDATE: Clovis Oncology Says Meeting With FDA To Discuss Plans For SNDA Submission For First-Line Maintenance Treatment For Women With Advanced Ovarian Cancer

By Michael Horton
July 6, 4:36 PM
-Reuters

CLVS

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Adverum Biotechnologies Completes IND Amendment And Prepares To Initiate The Phase 2 LUNA Trial Of ADVM-022 In Wet AMD

By Benzinga Newsdesk
July 6, 4:10 PM
- Cash runway extended into 2025 due to corporate restructuring to prioritize the clinical development of ADVM-022 and provide additional resources beyond anticipated one-year topline results of the Phase 2 LUNA trial -

ADVM

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6 minute read
  • FDA
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Global Coalition For Adaptive Research, Biohaven, And Vigeo Announce Commencement Of Biohaven’s Troriluzole And Vigeo’s VT1021 In GBM AGILE Trial

By Benzinga Newsdesk
July 6, 1:03 PM
Global Coalition for Adaptive Research, Biohaven, and Vigeo Announce Commencement of Biohaven's Troriluzole and Vigeo'S VT1021 in GBM AGILE Trial Biohaven and Vigeo Now Enrolling in GBM AGILE, Registrational

BHVN

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2 minute read
  • FDA
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Alterity Therapeutics Doses First Patient in ATH434 Phase 2 Clinical Trial in Multiple System Atrophy

By Benzinga Newsdesk
July 6, 11:00 AM
Alterity Therapeutics ((ASX: ATH, NASDAQ:ATHE) ("Alterity" or "the Company"), a biotechnology company dedicated to developing disease modifying treatments for neurodegenerative diseases, today

ATHE

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1 minute read
  • FDA
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NYC Healthy Tweets ‘Monkeypox vaccine doses have arrived in NYC! We plan to make appointments available starting

By Benzinga Newsdesk
July 6, 10:46 AM
https://twitter.com/nycHealthy/status/1544693903407955968

AEMD

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The Daily Biotech Pulse: FDA Decision On Biogen Alzheimer’s Drug Due In January, FDA Reviews Roche’s Lymphoma Candidate, Rare Pediatric Tag For Kazia’s Pediatric Brain Cancer Candidate

By Vandana Singh
July 6, 9:14 AM
Here's a roundup of top developments in the biotech space over the last 24 hours:

AMTI

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InflaRx’s Stock Gains Following FDA Fast Track Status To Skin Disease Drug

By Ragothaman Srinivasan
July 6, 8:53 AM
The US Food and Drug Administration (FDA) granted a Fast Track designation to InflaRx’s (NASDAQ: IFRX) lead candidate Vilobelimab for the treatment of ulcerative Pyoderma Gangrenosum (PG).

IFRX

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  • Biotech
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Applied Molecular Transport Announces Top-line Phase 2 Results From MARKET Combination Trial Of Oral AMT-101 In Patients With Moderate-to-Severe Ulcerative Colitis

By Benzinga Newsdesk
July 6, 8:05 AM
– Similar clinical remission rates observed of 31.8% (7/22) in patients receiving combination (AMT-101 and adalimumab) versus 33.3% (9/27) in patients receiving placebo plus adalimumab at week

AMTI

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3 minute read
  • Biotech
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Vera Therapeutics Completes Patient Enrollment In Phase 2b ORIGIN Clinical Trial Of Atacicept For The Treatment of IgA Nephropathy

By Bill Haddad
July 6, 7:31 AM
Vera Therapeutics, Inc. (NASDAQ:VERA), a late-stage biotechnology company focused on developing and commercializing transformative treatments for patients with serious immunological disease, today announced completion of

VERA

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