Latest News for: fda) approval

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FDA Approves Bezos’ Lab-Grown ‘Fish’ Without Any Safety Data

Principia Scientific 11 Aug 2025
Critics believe this move is part of a larger globalist agenda to control the world’s food supply .
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Kamada Announces FDA Approval of its Plasma Collection Center in Houston, Texas

Nasdaq Globe Newswire 11 Aug 2025
Food and Drug Administration (FDA) has approved the supplement to its existing Biologics License Application (BLA) for ...
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FDA Approval of its Plasma Collection Center in Houston, Texas (Kamada Ltd)

Public Technologies 11 Aug 2025
). The text version of this document is not available ... Disclaimer. Kamada Ltd.
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Thermo Fisher Receives FDA Approval for NGS-Based Companion Diagnostic for New Non-Small Cell Lung Cancer Treatment

The Galveston Daily News 11 Aug 2025
CARLSBAD, Calif.--(BUSINESS WIRE)--Aug 11, 2025-- ....
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First FDA-Approved Treatment for MacTel Performed

The Milton Standard Journal 11 Aug 2025
CUMBERLAND, R.I.--(BUSINESS WIRE)--Aug 11, 2025-- ....
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PharmaTher Announces FDA Approval of Ketamine (KETARx™)

The Eagle-Tribune 11 Aug 2025
TORONTO, Aug ... (the “Company” or “PharmaTher”) (OTCQB.
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FDA Approves Tiziana Life Sciences Phase 2 IND for Multiple System Atrophy

Nasdaq Globe Newswire 11 Aug 2025
Food & Drug Administration (FDA) have approved the IND for its Phase 2a clinical trial of intranasal foralumab in patients with ...
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Kamada Announces FDA Approval of its Plasma Collection Center in Houston, Texas (Form 6-K) (Kamada Ltd)

Public Technologies 11 Aug 2025
Kamada Announces FDA Approval of its Plasma Collection Center in Houston, Texas ● Houston Center Cleared to Commence Commercial Sales of Normal Source Plasma ... Following FDA's approval of the Houston ...
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ABSSSI Pipeline 2025: Detailed Clinical Trials and FDA-Approved Therapies Review By DelveInsight | Durata Therapeutics, ...

GetNews 11 Aug 2025
The funds will also be used to begin a Phase 3 ABSSSI trial in Australia, advance other clinical programs, support an IND submission to the FDA, and provide working capital.
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FDA Approves Tiziana Life Sciences Phase 2 IND for Multiple System Atrophy (Form 6-K) (Tiziana Life Sciences Ltd)

Public Technologies 11 Aug 2025
FDA Approves Tiziana Life Sciences Phase 2 IND for Multiple System Atrophy ... Food & Drug Administration (FDA) have approved the IND for its Phase 2a clinical trial of intranasal foralumab in patients with Multiple System Atrophy (MSA).
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Cytomegalovirus Infection Pipeline 2025: MOA, ROA, FDA-Approved Drugs, and Clinical Trial Progress Assessment by DelveInsight ...

GetNews 11 Aug 2025
The report also covers a detailed description of the drug, including the mechanism of action of the drug, clinical studies, NDA approvals (if any), and product development activities comprising the ...
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Now you don’t need reading glasses, new FDA-approved eye drops can sharpen near vision

The Times of India 09 Aug 2025
The US Food and Drug Administration has approved Vizz eye drops ... .
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Law enforcement agencies issuing letters for removal of non-FDA approved hemp products

The Clarksdale Press Register 09 Aug 2025
It states the sale of hemp products intended for human consumption or ingestion that are not FDA-approved is illegal, citing a issued by the Mississippi Attorney General’s Office ... The FDA has approved ...
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Orchestra BioMed Announces Rollout of FDA-Approved BACKBEAT Global Pivotal Study Protocol

Hastings Tribune 08 Aug 2025
FDA-approved protocol update significantly expands patient ...
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FDA Approves SetPoint Neuroimmune Modulation Device for Rheumatoid Arthritis

US News 08 Aug 2025
The implantable neurostimulation device activates the body's innate anti-inflammatory and immune-restorative pathways ... .

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