Drug News

Medindia's Press Release’ section provides the latest press release on Drug from across the world for the global audience. This page links to 12872 Drug press releases.

Kimer Med, innovative New Zealand biotech start-up, signs contract with Battelle Memorial Institute to pioneer antiviral drug advances

12 month contract focused on the development of new antiviral drugs Novel candidates to be produced using Kimer Med's broad-spectrum antiviral platform 95% of viral diseases lack an approved antiviral treatment Download high resolution ...


Good News--MS Drugs Taken While Breastfeeding May Not Affect Child Development

MINNEAPOLIS , March 4, 2024 /PRNewswire/ -- Certain medications for multiple sclerosis (MS) called monoclonal antibodies, taken while breastfeeding, may not affect the development of a child during the first three years of life, according ...

Caliway Announced Orphan Drug Designation Granted to CBL-514 for the Treatment of Dercum's Disease

-       CBL-514 is the first and only drug to receive both Orphan Drug Designation and Fast Track designation for Dercum's disease treatment. NEW TAIPEI CITY , March 3, 2024 /PRNewswire/ -- Caliway Biopharmaceuticals (Caliway) ...

Jacobio Pharma Receives IND Approval for P53 Y220C Activator JAB-30300 in the U.S.

BEIJING , SHANGHAI and BOSTON , March 1, 2024 /PRNewswire/ -- Jacobio Pharma (1167.HK), a clinical-stage oncology company drugging the undruggable targets, today announced it received IND (Investigational New Drug) approval of its ...

Innovent Announces First Participant Dosed in a Phase I Study of IBI3002 (an anti-IL-4Ra/TSLP bispecific antibody) in Australia

ROCKVILLE, Md. and SUZHOU, China , Feb. 29, 2024 /PRNewswire/ -- Innovent Biologics, Inc. (Innovent) (HKEX: 01801), a world-class biopharmaceutical company that develops, manufactures and commercializes high-quality medicines for the ...

LISCure Biosciences Announces FDA Clearance of IND Application to Initiate a Phase 2 Study of LB-P8 for Primary Sclerosing Cholangitis (PSC)

Represents first ever live biotherapeutic product to receive IND clearance for PSC Phase 2 clinical trial will evaluate the safety and efficacy, including clinical endpoints of LB-P8 SEONGNAM, South Korea , Feb. 29, 2024 /PRNewswire/ ...

This Rare Disease Day, Feb. 29, CORD celebrates the launch of the Canadian Rare Disease Network - but patients still have no access to the promised $1.4 billion in federal funds for rare disease drugs

The federal government promised a Rare Disease Drug Strategy five years ago and announced $1.4 billion in drug funding last March. Today  not a single patient has received a single penny from that fund , despite urgent unmet needs The ...

First product based on LTS Sorrel™ wearable drug delivery platform launched in the US

ANDERNACH, Germany , Feb. 28, 2024 /PRNewswire/ -- LTS LOHMANN Therapie-Systeme AG ("LTS"), a leading pharmaceutical technology company, announced today that its customer Coherus BioSciences, Inc ("Coherus") has launched its UDENYCA® on-body ...

Tilray Provides International Cannabis Update on Milestone German Cannabis Legalization

Germany’s De-Scheduling of Cannabis Opens Path to New Opportunities for Tilray in Potential $3bn Medical Market European Union Medical Cannabis Market Now Projected to Become $45bn NEW YORK and NEUMÜNSTER, Germany, Feb. 28, 2024 ...

Phylos® and People Science® Announce Results of IRB-Backed Controlled Research Study on the Energizing Effects of THCV

Launches Natural Natural™ ingredient brand to raise consumer awareness of naturally-derived rare cannabinoids PORTLAND, Ore. , Feb. 27, 2024 /PRNewswire/ -- Cannabis genetics company  Phylos ® , along with People  Science , a ...

Drug News »

US FDA Approval of N-803: Ray of Hope For Bladder Cancer Patients

US FDA Approval of N-803: Ray of Hope For Bladder Cancer Patients

The immunotherapy-boosting drug N-803, with the brand name Anktiva, was granted approval by the U.S. Food and Drug Administration (FDA) on April 22, 2024, based on the positive outcome of a clinical trial ...

Resmetirom For MASH: Approved by US FDA, Increase in Partnerships

Resmetirom For MASH: Approved by US FDA, Increase in Partnerships

Biopharmaceutical companies are once again competing in the development of innovative drugs for metabolic dysfunction-associated steatohepatitis (MASH), after a series of failures faced by drug manufacturers. The US FDA approval of ...

Semaglutide: A Dominant Player for Patients With Heart Failure

Semaglutide: A Dominant Player for Patients With Heart Failure

A study was presented by the Gardy Health system in Atlanta, Georgia, US, at the 73rd Annual Scientific Session of the American College of Cardiology. The study was conducted to evaluate the frequency of heart failure hospitalizations (HFH) in ...

Physician's Lack Agreement – Patients Prefer Branded or Generic Drugs?

Physician's Lack Agreement – Patients Prefer Branded or Generic Drugs?

Generic drugs and Branded drugs are essentially the same, as they both have the same active ingredient. Generic drugs can provide the same therapeutic advantages as branded drugs at a reduced cost, as they do not have to undergo extensive ...

Drug Resistant Melanoma Caused Due to Break in Genes!

Drug Resistant Melanoma Caused Due to Break in Genes!

Melanoma is an extremely fatal form of skin cancer and has inherent resistance to both radiotherapy and chemotherapy ( ). The occurrence of Melanoma has been increasing steadily and become a major health issue since the 5-year ...

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