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 12875 Drug press releases.

Cold and Flu Remedy Sales Increase by 30 Percent at Meijer Pharmacies

Another reminder that it's never too late to get a flu shot GRAND RAPIDS, Mich. , Jan. 9, 2017 /PRNewswire/ -- Meijer stores have experienced a 30 percent increase in cold and flu remedies being purchased over the counter at its pharmacies ...


Vanda Pharmaceuticals Reports Preliminary Fourth Quarter and Full Year 2016 Revenue Results and 2017 Financial Guidance

- 2016 Total revenues are expected to be approximately $146 million WASHINGTON , Jan. 9, 2017 /PRNewswire/ -- Vanda Pharmaceuticals Inc. (Vanda) (NASDAQ: VNDA), a biopharmaceutical company focused on the development and commercialization ...

inVentiv Health Spotlights Patient-Centered Innovations With The Potential To Accelerate Drug Delivery At Biotech Showcase™

Event Panels to Discuss Value of Real-World Evidence (RWE) and Digital Medicine BURLINGTON, Mass. , Jan. 8, 2017 /PRNewswire/ -- inVentiv Health, a global professional services organization designed to help the biopharmaceutical industry ...

Drug for Cholangiocarcinoma in Phase 1 Trial

(“RedHill” or the “Company”), a specialty biopharmaceutical company primarily focused on the development and commercialization of late clinical-stage, proprietary, orally-administered, small molecule drugs for gastrointestinal and inflammatory ...

Breckenridge Pharmaceutical, Inc. Announces Final ANDA Approval for Bendamustine HCl Powder for IV (Treanda®)

BOCA RATON, Fla. , Jan. 6, 2017 /PRNewswire/ -- Breckenridge Pharmaceutical, Inc. announced that FDA has granted final approval of its ANDA bendamustine hydrochloride powder for IV (infusion), 25 mg/vial and 100 mg/vial, a generic version ...

Guardant Health to create a new 500-plus-gene liquid biopsy panel with several leading pharmaceutical companies to accelerate clinical trials and drug development

REDWOOD CITY, Calif. , Jan. 6, 2017 /PRNewswire/ -- Guardant Health today announced that it has entered into separate agreements with AstraZeneca, Merck (known as MSD outside the United States and Canada ), Merck KGaA, Darmstadt, Germany ...

Impax Confirms Patent Challenge Relating to Generic Aubagio® (teriflunomide) Tablets, 14 mg

HAYWARD, Calif. , Jan. 6, 2017 /PRNewswire/ --  Impax Laboratories, Inc. (NASDAQ: IPXL) today confirmed that it has filed an Abbreviated New Drug Application (ANDA) with the U.S. Food & Drug Administration (FDA) containing a ...

RG7916 Granted Orphan Drug Designation in the U.S. for the Treatment of Spinal Muscular Atrophy

SOUTH PLAINFIELD, N.J. , Jan. 6, 2017 /PRNewswire/ -- PTC Therapeutics, Inc. (NASDAQ: PTCT) today announced that the U.S. Food and Drug Administration (FDA) has granted orphan drug designation (ODD) to RG7916 for the treatment of patients ...

CEO Of Leading Regenerative Medicine Company, ORIG3N, To Present At Biotech Showcase

BOSTON , Jan. 6, 2017 /PRNewswire/ -- ORIG3N Inc., a Boston -based biomedical research company, announced today that its CEO, Robin Y. Smith , will present a company overview at the 9th Annual Biotech Showcase . The presentation will take ...

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Dapagliflozin: A Potential Aid in Acute Heart Failure

Dapagliflozin: A Potential Aid in Acute Heart Failure

Dapagliflozin, a medication prescribed for managing Type 2 diabetes , has demonstrated additional benefits in heart failure conditions. This drug lowers the likelihood of hospitalization due to heart failure and mortality in ...

Harnessing mRNA Vaccine Technology for Disease Prevention

Harnessing mRNA Vaccine Technology for Disease Prevention

The efficacy of mRNA vaccine technology demonstrated during the COVID-19 pandemic provides optimism for its utilization in mitigating preventable illnesses across various disease domains ( ). ...

Lower Dose MPox Vaccine: Safe With Equal Six-Week Antibody Response

Lower Dose MPox Vaccine: Safe With Equal Six-Week Antibody Response

An intradermal monkeypox (Mpox) vaccination regimen with reduced dosage proved safe and elicited an antibody response comparable to the standard regimen at six weeks (two weeks post-second dose). ...

Cholera Oral Vaccine: WHO Prequalifies a New Simplified Vaccine

Cholera Oral Vaccine: WHO Prequalifies a New Simplified Vaccine

The World Health Organization (WHO) granted prequalification to a novel oral cholera vaccine on April 12. The Euvichol-S oral vaccine, which is inactivated, demonstrates comparable effectiveness to the current vaccines, ...

Alectinib: Adjuvant Treatment for Lung Cancer Approved by US FDA

Alectinib: Adjuvant Treatment for Lung Cancer Approved by US FDA

Alectinib, a molecule developed by Genentech, Inc has been granted approval by the Food and Drug Administration on April 18, 2024, for the adjuvant treatment of patients with anaplastic lymphoma kinase (ALK)-positive non-small cell lung cancer ...

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