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Government Administration Activities

STRATA Skin Sciences
Regional

STRATA Skin Sciences Gains Approval for Advanced Laser Device in Japan

July 24, 2024July 23, 2024 - by Timothy Alexander

HORSHAM, PA — STRATA Skin Sciences, Inc. (NASDAQ: SSKN) has secured approval from Japan’s Ministry of Health, Labor, and Welfare for its XTRAC Momentumâ„¢ 1.0 device. This advanced excimer laser, …

STRATA Skin Sciences Gains Approval for Advanced Laser Device in Japan Read More

Marinus Pharmaceuticals
Regional

Marinus Pharmaceuticals Gains Approval for Seizure Drug in China

July 23, 2024July 22, 2024 - by Timothy Alexander

RADNOR, PA — Marinus Pharmaceuticals, Inc. (Nasdaq: MRNS) has announced that China’s National Medical Products Administration (NMPA) has approved its ganaxolone oral suspension. This drug targets epileptic seizures in patients …

Marinus Pharmaceuticals Gains Approval for Seizure Drug in China Read More
Passage Bio
Health / Medical / Regional

Passage Bio Receives FDA Support for Expanding Dementia Treatment Trial

July 17, 2024July 16, 2024 - by Timothy Alexander

PHILADELPHIA, PA — Passage Bio, Inc. (NASDAQ: PASG) announced positive feedback from the U.S. Food and Drug Administration (FDA) on its proposal to evaluate PBFT02 for treating frontotemporal dementia (FTD) …

Passage Bio Receives FDA Support for Expanding Dementia Treatment Trial Read More

INOVIO Pharmaceuticals
Regional

INOVIO’s DNA Medicine INO-3107 Receives U.K. Innovation Passport

July 15, 2024July 14, 2024 - by Timothy Alexander

PLYMOUTH MEETING, PA — INOVIO (NASDAQ: INO) announced that its lead DNA medicine candidate, INO-3107, has been granted an Innovation Passport by the U.K.’s Innovative Licensing and Access Pathway (ILAP). …

INOVIO’s DNA Medicine INO-3107 Receives U.K. Innovation Passport Read More
Cat
National

FDA Approves First Generic Methimazole Oral Solution for Cats

July 14, 2024July 14, 2024 - by Maryann Pugh

WASHINGTON, D.C. — The U.S. Food and Drug Administration (FDA) recently approved Felanorm, the first generic methimazole oral solution for treating hyperthyroidism in cats. This new medication offers a vital …

FDA Approves First Generic Methimazole Oral Solution for Cats Read More

United States Department of Labor
National / Social Services

U.S. Department of Labor Awards $56 Million to Aid Reentry for Formerly Incarcerated Individuals

July 8, 2024July 8, 2024 - by Maryann Pugh

WASHINGTON, D.C. — The U.S. Department of Labor announced the award of more than $56 million in grants aimed at reducing recidivism and assisting individuals re-entering their communities after incarceration. …

U.S. Department of Labor Awards $56 Million to Aid Reentry for Formerly Incarcerated Individuals Read More
Technology
National / Technology

U.S. Commerce Department Awards $504 Million to Boost Tech Hubs Nationwide

July 8, 2024July 8, 2024 - by Maryann Pugh

WASHINGTON, D.C. — The U.S. Department of Commerce’s Economic Development Administration (EDA) recently announced a new round of funding totaling approximately $504 million. These implementation grants aim to scale up …

U.S. Commerce Department Awards $504 Million to Boost Tech Hubs Nationwide Read More

Diamond Shruumz-brand products
National

FDA Warns Against Diamond Shruumz-brand Chocolate Bars, Cones, and Gummies Amid Illness Outbreak

June 23, 2024June 23, 2024 - by Maryann Pugh

WASHINGTON, D.C. — The U.S. Food and Drug Administration (FDA) recently updated its advisory regarding illnesses linked to Diamond Shruumz-brand Chocolate Bars, Cones, and Gummies. As of June 17, 2024, …

FDA Warns Against Diamond Shruumz-brand Chocolate Bars, Cones, and Gummies Amid Illness Outbreak Read More
FDA
Health / Medical / National

FDA Broadens Approval of Elevidys Gene Therapy for Duchenne Muscular Dystrophy Patients

June 22, 2024June 21, 2024 - by Maryann Pugh

WASHINGTON, D.C. — This week, in a significant step for the medical world and hope for patients, the U.S. Food and Drug Administration expanded the approval of Elevidys, a gene …

FDA Broadens Approval of Elevidys Gene Therapy for Duchenne Muscular Dystrophy Patients Read More
Medical news
Cancer / National

FDA Approves Keytruda Combination for Advanced Endometrial Cancer

June 20, 2024June 20, 2024 - by Maryann Pugh

WASHINGTON, D.C. — On Monday, the Food and Drug Administration (FDA) approved pembrolizumab (Keytruda, Merck) in combination with carboplatin and paclitaxel, followed by single-agent pembrolizumab, for adult patients with primary …

FDA Approves Keytruda Combination for Advanced Endometrial Cancer Read More

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