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Government Administration Activities

U.S. Food and Drug Administration (FDA)
Regional

FDA Approves Rapiblyk for Pediatric SVT Patients in U.S.

April 27, 2026April 27, 2026 - by Timothy Alexander

WILMINGTON, DE — The U.S. Food and Drug Administration recently approved RAPIBLYK® (landiolol) for pediatric patients from birth to under 18 years old with supraventricular tachycardia, expanding its use beyond …

FDA Approves Rapiblyk for Pediatric SVT Patients in U.S. Read More

Medical research
Regional

Medicus Pharma Submits Orphan Drug Application for SkinJect

April 22, 2026April 21, 2026 - by Timothy Alexander

PHILADELPHIA, PA — Medicus Pharma Ltd. (NASDAQ: MDCX) said it submitted an Orphan Drug Designation application to the U.S. Food and Drug Administration for SkinJect (D-MNA) to treat basal cell …

Medicus Pharma Submits Orphan Drug Application for SkinJect Read More
Arbutus Biopharma
Regional

Arbutus Drug Candidate Receives FDA Fast Track Designation

April 22, 2026April 20, 2026 - by Timothy Alexander

WARMINSTER, PA — Arbutus Biopharma Corporation (Nasdaq: ABUS) announced that the U.S. Food and Drug Administration has granted Fast Track designation to its drug candidate imdusiran for the treatment of …

Arbutus Drug Candidate Receives FDA Fast Track Designation Read More

Pennsylvania Aggregates and Concrete Association
Pennsylvania

PACA, EPA Region 3 Sign Agreement on Environmental Collaboration

April 21, 2026April 20, 2026 - by Timothy Alexander

HARRISBURG, PA — The Pennsylvania Aggregates and Concrete Association has signed a memorandum of understanding with the U.S. Environmental Protection Agency Region 3 to expand collaboration on environmental practices and …

PACA, EPA Region 3 Sign Agreement on Environmental Collaboration Read More
NRx Pharmaceuticals
Regional

NRx Receives FDA Feedback on Ketamine Drug Labeling

April 13, 2026April 13, 2026 - by Timothy Alexander

WILMINGTON, DE — NRx Pharmaceuticals Inc. (Nasdaq: NRXP) recently received preliminary feedback from the U.S. Food and Drug Administration on labeling for its preservative-free ketamine product, as the company continues …

NRx Receives FDA Feedback on Ketamine Drug Labeling Read More

FORE Biotherapeutics
Regional

FDA Grants Breakthrough Status to Fore Bio Brain Cancer Drug

April 12, 2026April 11, 2026 - by Timothy Alexander

PHILADELPHIA, PA — The U.S. Food and Drug Administration recently granted Breakthrough Therapy Designation to plixorafenib, an investigational drug from FORE Biotherapeutics, for the treatment of adults with BRAF V600E-mutated …

FDA Grants Breakthrough Status to Fore Bio Brain Cancer Drug Read More
Oil and gas energy
National

Interior Merges Offshore Agencies to Boost Oversight Efficiency

April 6, 2026April 5, 2026 - by Maryann Pugh

WASHINGTON, D.C. — Federal officials are restructuring offshore energy oversight by combining two key agencies into a single entity aimed at improving coordination and decision-making.

Interior Merges Offshore Agencies to Boost Oversight Efficiency Read More

Hamilton Lane
Regional

Hamilton Lane Launches Credit Income Fund for Private Wealth Investors

April 5, 2026April 4, 2026 - by Timothy Alexander

CONSHOHOCKEN, PA — Hamilton Lane (Nasdaq: HLNE) recently received regulatory approval from the U.S. Securities and Exchange Commission for its Hamilton Lane Credit Income Fund, a new private credit vehicle …

Hamilton Lane Launches Credit Income Fund for Private Wealth Investors Read More
Weight loss
Health / Medical / National

FDA Fast-Tracks New Weight-Loss Drug in Record Time

April 5, 2026April 4, 2026 - by Maryann Pugh

WASHINGTON, D.C. — A new weight-loss drug is now available months ahead of schedule after the U.S. Food and Drug Administration approved Foundayo (orforglipron) in just 50 days, marking one …

FDA Fast-Tracks New Weight-Loss Drug in Record Time Read More
iECURE
Regional

FDA Selects iECURE Therapy for Manufacturing Readiness Pilot Program

April 2, 2026April 1, 2026 - by Timothy Alexander

PHILADELPHIA, PA — iECURE said the U.S. Food and Drug Administration has selected ECUR-506, the company’s investigational gene insertion therapy for neonatal-onset ornithine transcarbamylase deficiency, for the agency’s Chemistry, Manufacturing, …

FDA Selects iECURE Therapy for Manufacturing Readiness Pilot Program Read More

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