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Amgen announces top-line CLARION trial results

American Pharmacy News Reports | Sep 29, 2016
Amgen has announced positive results from its CLARION trial.

Amgen recently reported top-line results of its Phase 3 CLARION trial that was designed to assess KYPROLIS (carfilzomib), melphalan and prednisone (KMP), Amgen's new investigational regimen, while comparing it to Velcade (bortezomib). Read More »

Tarix Orphan receives Orphan Drug Status for TXA127 from FDA

American Pharmacy News Reports | Sep 28, 2016
The FDA has granted Orphan Drug Status to Tarix Orphan for TXA127.

Tarix Orphan LLC recently announced that the U.S. Food and Drug Administration (FDA) has granted Orphan Drug Status to TXA127, the company’s prospective treatment for Recessive Dystrophic Epidermolysis Bullosa (RDEB), a rare genetic skin disorder. Read More »

Armetheon releases results of Phase 1 tecarfarin trial

American Pharmacy News Reports | Sep 28, 2016
Armetheon has released the results of its Phase 1 tecarfarin clinical trial.

Armetheon Inc., a specialty pharmaceutical company that focuses on the development of novel small molecule drugs for the treatment of cardiovascular diseases, recently released the results of its Phase 1 clinical trial assessing how the pharmacokinetics (PK) of tecarfarin and of warfarin is affected by severe chronic kidney disease (CKD). Read More »

NAMZARIC now available in prescription in U.S.

American Pharmacy News Reports | Sep 28, 2016
NAMZARIC is now available through prescriptions in the U.S.

Allergen plc recently announced that NAMZARIC is now available through prescription in pharmacies across the United States. Read More »

EMA accepts Mylan, Biocon MAA for Trastuzumab for review

American Pharmacy News Reports | Sep 28, 2016
Mylan and Biocon's MAA for Trastuzumab has been accepted for review by the EMA.

Mylan N.V. and Biocon Ltd. recently announced that Mylan’s Marketing Authorization Application (MAA) for Trastuzumab has been accepted by the European Medicines Agency (EMA) for review.  Read More »

PharmaMar submits MAA for Aplidin to EMA

American Pharmacy News Reports | Sep 27, 2016
PharmaMar has submitted an Marketing Authorization Application to the EMA for Aplidin.

PharmaMar recently submitted a Marketing Authorization Application (MAA) for Aplidin to the European Medicines Agency (EMA). Read More »

PCMA President and CEO testifies on drug abuse before House Subcommittee

American Pharmacy News Reports | Sep 27, 2016
PCMA President and CEO Mark Merritt testified before a House Subcommittee to make recommendations on drug abuse.

Mark Merritt, president and CEO of the Pharmaceutical Care Management Association (PCMA), recently testified before the House Judiciary Subcommittee on Regulatory Reform, Commercial and Antitrust Law. Read More »

Meridian launches ASR product line

American Pharmacy News Reports | Sep 27, 2016
Meridian has launched its new line of ASR products.

Meridian Bioscience Inc. has officially launched its Analyte Specific Reagent (ASR) line of products. Read More »

Medivir releases MIV-711-201 trial data

American Pharmacy News Reports | Sep 27, 2016
Medivir recently released data from its Phase IIa MIV-711-201 trial.

Medivir AB announced last week the release of new data from its Phase IIa MIV-711-201 trial. Read More »

Faraday announces start of FDY-5301 study

American Pharmacy News Reports | Sep 26, 2016
Faraday has announced the start of the FDY-5301 trial.

Faraday Pharmaceuticals recently announced the start of its FDY-5301 Phase 1 clinical study, which is designed to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of FDY-5301, the company’s lead compound. Read More »

Portola submits MMA to EMA for IndexXa

American Pharmacy News Reports | Sep 26, 2016
Portola is seeking approval for IndexXa from the European Union.

Portola Pharmaceuticals Inc. recently announced it has submitted a Marketing Authorization Application (MAA) for IndexXa to the European Medicines Agency, noting that the validation period has been completed and it has been accepted for review. Read More »

AbbVie releases new GARNET trial data

American Pharmacy News Reports | Sep 26, 2016
AbbVie has released new data regarding its Phase 3 GARNET trial.

AbbVie recently released new data from its Phase 3 GARNET study involving the combination of VIEKIRAX and EXVIERA that shows significant response rates after only eight weeks of the medication. Read More »

AcelRx presents SAP301 data at annual ASPS meeting

American Pharmacy News Reports | Sep 26, 2016
AcelRx recently presented the analysis of the SAP301 trial at the ASPS annual meeting.

AcelRx Pharmaceuticals Inc. recently presented the subgroup analysis from the SAP301 clinical study by board-certified plastic surgeon and AcelRx clinical investigator Dr. Shankar Lakshman at the American Society of Plastic Surgeons (ASPS) annual meeting. Read More »

Johnson & Johnson commits to advancement of world health

American Pharmacy News Reports | Sep 23, 2016
Johnson & Johnson has committed itself to the advancement of world health.

Johnson & Johnson recently made a five-year commitment to aid the United Nations Sustainable Development Goals in its mission to see the improvement of the health and well-being of people worldwide. Read More »

Neuraltus announces beginning of second NP001 Phase 2 trial

American Pharmacy News Reports | Sep 23, 2016
Neuraltus has announced the beginning of a second NP001 Phase 2 trial.

Neuraltus Pharmaceuticals Inc. recently announced that it has begun a second Phase 2 trial of NP001, its investigational treatment designed for patients who have amyotrophic lateral sclerosis (ALS), or Lou Gehrig’s disease. Read More »

Two Akcea clinical trial results published in The Lancet

American Pharmacy News Reports | Sep 23, 2016
Akcea has announced the publication of two clinical trial results in The Lancet.

Akcea Therapeutics, an Ionis Pharmaceuticals subsidiary, recently reported that significant results from two clinical studies of INOIS-APO(a) and IONIS-APO(a)-L have been published in The Lancet. Read More »

FDA approves Lannett’s ANDA for Buprenorphine and Naloxone Sublingual Tablets

American Pharmacy News Reports | Sep 22, 2016
The FDA has approved Lannett's ANDA for Buprenorphine and Naloxone Sublingual Tablets.

Lannett Company Inc. announced that the U.S. Food and Drug Administration (FDA) recently approved its Abbreviated New Drug Application (ANDA) for Buprenorphine and Naloxone Sublingual Tablets for the dosing options of 2 mg/0.5 mg and 8 mg/2mg. Read More »

Upsher-Smith announces exclusive agreement with emerging pharmaceutical company

American Pharmacy News Reports | Sep 22, 2016
Upsher-Smith has announced an exclusive agreement with an emerging pharmaceutical company.

Upsher-Smith Laboratories Inc. recently announced it has entered into an exclusive agreement with an emerging pharmaceutical company for the marketing and distribution of a generic central nervous system (CNS) product. Read More »

Valeant announces new leadership team roles

American Pharmacy News Reports | Sep 22, 2016
Valeant has announces changes to its leadership team.

Valeant Pharmaceuticals International has appointed of Paul S. Herendeen as the company’s new EVP of Finance. Read More »

Crown BioScience NAFLD model in development

American Pharmacy News Reports | Sep 22, 2016
Crown BioScience is developing a non-alcoholic fatty liver disease model.

Crown BioScience recently reported that it is currently developing a non-alcoholic fatty liver disease (NAFLD) model. Read More »

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