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MatrixCare acquires long-term EHR provider SigmaCare

American Pharmacy News Reports | Jun 27, 2017
SigmaCare customers have full access to MatrixCare’s resources.

Population health management logistics just became easier for collective clients of two health-care administrative providers with MatrixCare’s acquisition of electronic health record (EHR) firm SigmaCare in the metropolitan New York area. Read More »

PharmaMar to present findings to FDA's Pediatric Oncology Subcommittee

American Pharmacy News Reports | Jun 27, 2017
PharmaMar officials believe there may be potential relevance for PM1183 to be developed in one or more pediatric cancers.

PharmaMar will present clinical data from Phase I and II studies examining Zepsyre’s effect on pediatric cancers and hematological disorders to the Pediatric Oncology Subcommittee of the Oncologic Drugs Advisory Committee of the U.S. Food and Drug Administration. Read More »

Immune Pharmaceuticals enrolls patients in trial for CMML drug

American Pharmacy News Reports | Jun 27, 2017
The trial will involve 15 adult patients with CMM who will receive Ceplene in conjunction with low-dose Proleukin.

Immune Pharmaceuticals is enrolling patients in a Phase I and II clinical trial that will determine the safety and efficacy levels of Ceplene as a treatment for Chronic Myelomonocytic Leukemia. Read More »

ANI Pharmaceuticals launches pair of diarrhea treatments in U.S.

American Pharmacy News Reports | Jun 27, 2017
ANI’s entrance into the market adds a third generic competitor.

ANI Pharmaceuticals Inc. recently made its U.S. launch of Diphenoxylate HCl and Atropine Sulfate Tablet to treat diarrhea. Read More »

Do Trial Lawyer Rx Drug Ads Scare Patients from Taking Medications? (SPONSORED)

American Pharmacy News Reports | Jun 26, 2017

One in four Americans taking certain prescribed medicines say they would stop taking them immediately—without consulting their doctor—after seeing ads promoting lawsuits against the drugs’ manufacturers, according to a new national survey released by the U.S. Chamber Institute for Legal Reform (ILR). Read More »

Imaging3 contracts Intertek to manage FDA guidance protocols

American Pharmacy News Reports | Jun 25, 2017
Intertek will make sure the Dominion VI product meets quality, health, environmental, safety and social accountability standards.

Imaging3 Inc. has hired Intertek Inc. to oversee hazard analytics and U.S. Federal Drug Administration guidance protocols during the submission of the company’s Dominion VI imaging device with patented SmartScan 3D technology. Read More »

Seattle Genetics submits BLA for lymphoma treatment

Mark Iandolo | Jun 25, 2017
Adcetris treats patients with cutaneous T-cell lymphoma.

Seattle Genetics Inc. has submitted a Biologics License Application (BLA) to the U.S. Food and Drug Administration using data from its recent Phase 3 Alcanza trial and two Phase 2 investigator-sponsored trials of Adcetris. Read More »

Indiana optometrists open ‘Little Eyes’ just for kids

American Pharmacy News Reports | Jun 25, 2017
The owners of

With its identity coined by the founding optometrist’s own child, RevolutionEYES’ “Little Eyes” recently opened in Carmel, Indiana, launching a pediatric eye care clinic caring for youngsters between 6 months and 13 years old. Read More »

Biohaven receives Fast Track Designation for SCA treatment

American Pharmacy News Reports | Jun 25, 2017
Currently, no medications are approved for the treatment of SCA.

Biohaven Pharmaceutical Holding Co. has been granted Fast Track Designation for its product candidate Trigriluzole by the FDA. Read More »

Churchill expands Commercial Leadership Team

American Pharmacy News Reports | Jun 25, 2017
Churchill Pharmaceuticals has expanded its Commercial Leadership Team.

Churchill Pharmaceuticals has expanded its Commercial Leadership Team. Read More »

QuVa Pharma rallies to address antacid shortage

American Pharmacy News Reports | Jun 23, 2017
QuVa Pharma's name derives from “Quality and Innovation.”

Addressing a recently reported nationwide antacid scarcity, QuVa Pharma Inc. — specializing in critical drug shortage products — has rallied with supplies of its own pharmaceutical quality sodium bicarbonate formulation at the ready for U.S. hospital distribution. Read More »

Lannett’s generic influenza drug wins FDA approval

American Pharmacy News Reports | Jun 23, 2017
The product is used to stem infection from some strains of influenza A.

To combat certain types of influenza, Lannett Co. Inc. can now market its Amantadine Hydrochloride Capsules USP in 100 mg. dose form following Food and Drug Administration approval of its Abbreviated New Drug Application. Read More »

Lannett gets FDA approval for extended-release niacin tabs

American Pharmacy News Reports | Jun 23, 2017
The product is available in both 500-mg. and 1000-mg. tablet doses.

Philadelphia-based Lannett Company Inc. recently obtained approval from the U.S. Food and Drug Administration (FDA) for its generic formulation of niacin in extended-release form, with the product available in both 500-mg and 1000-mg tablet doses. Read More »

Amgen presents 19 scientific abstracts to American Headache Society

American Pharmacy News Reports | Jun 23, 2017
Amgen also delivered the results from two Phase 3 studies of the drug.

Amgen recently presented 19 scientific abstracts at the 59th Annual Scientific Meeting of the American Headache Society, which took place in Boston. Read More »

OncoSec's melanoma drug receives Orphan Drug Designation

American Pharmacy News Reports | Jun 23, 2017
Tavokinogene telsaplasmid is the active biologic agent in ImmunoPulse IL-12, OncoSec’s lead product candidate.

OncoSec Medical Inc.'s pIL-12 drug, also known as tavokinogene telsaplasmid, has been given an Orphan Drug Designation by the U.S. Food and Drug Administration. Read More »

FDA to review oncology drug from Amgen and Allergan

American Pharmacy News Reports | Jun 22, 2017
In the Phase 3 study analyzing the biosimilar’s performance in treating patients with non-squamous non-small cell lung cancer, the drug met its primary endpoint.

Amgen and Allergan's data supporting their Biologics License Application for ABP 215, a biosimilar candidate to Avastin (bevacizumab), will be reviewed by the Oncologic Drugs Advisory Committee of the U.S. Food and Drug Administration by July 13. Read More »

AbbVie concludes Phase 3 study evaluating rheumatoid arthritis drug

American Pharmacy News Reports | Jun 22, 2017
After 12 weeks of treatment, upadacitinib met the primary endpoints.

AbbVie recently announced positive top-line results from its Phase 3 Select-Next trial, which evaluated upadacitinib as a treatment for rheumatoid arthritis patients. Read More »

SpePham AG to commercialize Navidea's Lymphoseek in Europe

American Pharmacy News Reports | Jun 22, 2017
The drug targets lymph nodes, the most likely place for cancer cells to spread from a primary tumor.

Navidea Biopharmaceuticals Inc. recently announced that SpePharm AG has launched Lymphoseek in the Denmark, the Netherlands and the United Kingdom. Read More »

Cigna, CVS partner to form Cigna HealthWorks

American Pharmacy News Reports | Jun 22, 2017
The program will deliver personalized pharmacy support, contracted discounts at CVS MinuteClinic, and a CVS ExtraCare Health card.

Cigna and CVS Health have launched Cigna HealthWorks, a partnership that brings Cigna benefits to CVS Pharmacy and CVS MinuteClinic retail health care centers. Read More »

Acorda updates tozadenant data at MDS Congress

American Pharmacy News Reports | Jun 22, 2017
Acorda anticipates results from a current Phase 3 clinical trial of the medication in early 2018.

Ardsley, New York-based biopharmaceutical firm Acorda Therapeutics revealed new information derived from clinical and preclinical studies of tozadenant at the recent 2017 International Congress of Parkinson’s Disease and Movement Disorders (MDS) in Vancouver, British Columbia. Read More »

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