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Biotechnology

Food and Drug Administration
Health / Medical / National

FDA Clears Faster Path for Gene Cures as Rare Disease Breakthrough Arrives

January 18, 2026January 18, 2026 - by Maryann Pugh

WASHINGTON, D.C. — The U.S. Food and Drug Administration signaled a sweeping shift in how cutting-edge therapies reach patients this month, unveiling regulatory flexibility for cell and gene therapies, modernizing …

FDA Clears Faster Path for Gene Cures as Rare Disease Breakthrough Arrives Read More

Syringes
Health / Medical / Pennsylvania

Pennsylvania Reaffirms Childhood Vaccine Access as Misinformation Swirls

January 13, 2026January 12, 2026 - by Maryann Pugh

HARRISBURG, PA — Pennsylvania health officials moved to calm growing anxiety over childhood vaccinations on Thursday, reaffirming that there have been no changes to vaccine access, insurance coverage, or school …

Pennsylvania Reaffirms Childhood Vaccine Access as Misinformation Swirls Read More
Aclaris Therapeutics
Public Companies

Aclaris Joins Nasdaq Biotech Index, Marking Milestone for Clinical-Stage Firm

December 24, 2025December 22, 2025 - by Timothy Alexander

WAYNE, PA — Aclaris Therapeutics, Inc. (NASDAQ: ACRS) said it has been added to the Nasdaq Biotechnology Index, a move that places the clinical-stage biopharmaceutical company among a select group …

Aclaris Joins Nasdaq Biotech Index, Marking Milestone for Clinical-Stage Firm Read More

Gene
Health / Medical / National

FDA Greenlights First Gene Therapy for Older SMA Patients, Raising Hope Nationwide

November 29, 2025November 29, 2025 - by Maryann Pugh

WASHINGTON, D.C. — The U.S. Food and Drug Administration approved Itvisma, a new adeno-associated virus vector-based gene therapy for spinal muscular atrophy, extending treatment eligibility to adults and children 2 …

FDA Greenlights First Gene Therapy for Older SMA Patients, Raising Hope Nationwide Read More
Medical research
Government / National

New Bipartisan Push Aims to Secure U.S. Lead in Biotech Manufacturing

November 20, 2025November 19, 2025 - by Maryann Pugh

WASHINGTON, D.C. — A bipartisan coalition in Congress is moving to strengthen America’s biotechnology and biopharmaceutical manufacturing base with the introduction of the Biomanufacturing Excellence Act — a sweeping proposal …

New Bipartisan Push Aims to Secure U.S. Lead in Biotech Manufacturing Read More

Latus Bio
Regional

Biotech Breakthrough: Latus Bio Doubles Down on AI to Revolutionize Gene Therapy

November 15, 2025November 13, 2025 - by Timothy Alexander

PHILADELPHIA, PA — Latus Bio, Inc. unveiled a significant expansion of its artificial intelligence and machine learning program as the company pushes deeper into AI-driven AAV capsid and payload design. …

Biotech Breakthrough: Latus Bio Doubles Down on AI to Revolutionize Gene Therapy Read More
Argosy Healthcare Partners
Strategic Combinations

Argosy Healthcare Partners Backs IS Benefits in Strategic Recapitalization Deal

November 14, 2025November 12, 2025 - by Timothy Alexander

WAYNE, PA & HOOKSETT, NH — Argosy Healthcare Partners (AHP) announced a recapitalization and strategic partnership with Integrated Solutions for Benefits and Insurance Services (IS Benefits), a New Hampshire–based firm …

Argosy Healthcare Partners Backs IS Benefits in Strategic Recapitalization Deal Read More

US Department of Health and Human Services (HHS)
Regional

HHS Issues Guidance Reaffirming Religious Exemptions in Vaccines for Children Program

September 6, 2025September 5, 2025 - by Timothy Alexander

WASHINGTON, D.C. — The U.S. Department of Health and Human Services (HHS) Office for Civil Rights has issued a nationwide letter reminding states that participation in the federal Vaccines for …

HHS Issues Guidance Reaffirming Religious Exemptions in Vaccines for Children Program Read More
Food and Drug Administration
Health / Medical / National

FDA Clears Path for Resumed Use of Elevidys Gene Therapy in Ambulatory DMD Patients

August 3, 2025August 3, 2025 - by Maryann Pugh

WASHINGTON, D.C. — The U.S. Food and Drug Administration (FDA) has recommended lifting the voluntary clinical hold on Elevidys for ambulatory patients with Duchenne Muscular Dystrophy (DMD), following a thorough …

FDA Clears Path for Resumed Use of Elevidys Gene Therapy in Ambulatory DMD Patients Read More
U.S. Food and Drug Administration
National / Research

FDA Shuts Down Sarepta Gene Therapy Trials After Three Deaths Linked to Liver Failure

July 21, 2025July 20, 2025 - by Maryann Pugh

WASHINGTON, D.C. — The U.S. Food and Drug Administration on Friday placed Sarepta Therapeutics’ gene therapy trials for limb girdle muscular dystrophy on clinical hold following the deaths of three patients …

FDA Shuts Down Sarepta Gene Therapy Trials After Three Deaths Linked to Liver Failure Read More

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