USFDA - HealthQuill

US-based Verrica Pharmaceuticals, a dermatology therapeutics company, has got FDA approval for a drug to treat a contagious viral skin disease, the company announced.

USFDA green lights Verrica’s drug to treat contagious viral skin disease

HQ Team July 24, 2023: US-based Verrica Pharmaceuticals, a dermatology therapeutics company, has got FDA approval for a drug to treat a contagious.

by HealthQuill
July 24, 2023
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Eli Lilly’s Alzheimer’s experimental drug, donanedab, slowed down cognitive and functional decline in people with early symptoms of the disease, according to a company statement.

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Eli Lilly: Alzheimer’s test drug slows cognitive decline in early stages

HQ Team July 18, 2023: Eli Lilly’s Alzheimer’s experimental drug, donanedab, slowed down cognitive and functional decline in people with early symptoms of.

by HealthQuill
July 18, 2023
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BridgeBio Pharma Inc., a Palo Alto, California-based biopharmaceutical company, reported its late-stage trial oral drug to treat a rare heart disease condition has yielded positive results.

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BridgeBio says oral drug to treat rare heart disease meets trial goal

HQ Team July 17, 2023: BridgeBio Pharma Inc., a Palo Alto, California-based biopharmaceutical company, reported its late-stage trial oral drug to treat a.

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July 17, 2023
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Granules India gets FDA nod for bio equivalent of Advil

HQ Team July 15, 2023: Granules India Limited, an Indian vertically integrated, high-growth pharmaceutical product manufacturing company, has got the US Food &.

by HealthQuill
July 15, 2023
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The FDA has approved the first daily oral contraceptive pill, Opill, without prescription to be sold in the US, according to a statement from the regulator.

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USFDA allows first oral contraceptive without a prescription

HQ Team July 14, 2023: The FDA has approved the first daily oral contraceptive pill, Opill, without prescription to be sold in the.

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July 14, 2023
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The FDA has told e-cigarette maker Fontem US, LLC, not to market or distribute its product myblu menthol in the US as it did not provide any “added benefits.”

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FDA bans Fontem US from selling e-cigarette myblu menthol

HQ Team July 11, 2023: The FDA has told e-cigarette maker Fontem US, LLC, not to market or distribute its product myblu menthol.

by HealthQuill
July 11, 2023
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The USFDA has granted a standard approval for Eisai and Biogen's Alzheimer injection, Leqembi —the first treatment to secure the traditional approval, paving the way for wider insurance coverage of the drug.

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USFDA grants green light to Eisai, Biogen’s Alzheimer’s drug Leqembi

HQ Team July 7, 2023: The USFDA has granted a standard approval for Eisai and Biogen’s Alzheimer injection, Leqembi —the first treatment to secure the.

by HealthQuill
July 7, 2023
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Artificial sweetener, sucralose, is “genotoxic” as it breaks up the DNA and also causes damage to the gut lining or leaky gut, a study reveals.

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Artificial sweetener sucralose breaks up DNA, may cause ‘leaky gut’

HQ Team June 30, 2023: Artificial sweetener, sucralose, is “genotoxic” as it breaks up the DNA and causes damage to the gut lining.

by HealthQuill
June 30, 2023
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Pfizer Inc. announced that USFDA has accepted its biologics license application for treating bleeding disorders in adults through gene therapy.

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FDA, EMA accept Pfizer’s BLP application for hemophilia therapy

HQ Team June 26, 2023: Pfizer Inc. announced that USFDA has accepted its biologics license application for treating bleeding disorders in adults through.