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Express Scripts expands program to limit opioid prescriptions

John Breslin | Aug 18, 2017
One in five users who start on a 10-day supply of opioid medication become long-term users.

Express Scripts, one of the largest pharmacy benefit managers (PBMs) in the country, has announced the expansion of a pilot program that limits opioid prescriptions to seven days without prior authorization. Read More »

Innovus Pharma orders 220,000 units of FlutiCare for product launch

American Pharmacy News Reports | Aug 17, 2017
FlutiCare, an over-the-counter fluticasone propionate nasal spray, treats patients with allergies.

Innovus Pharmaceuticals has ordered 220,000 units of FlutiCare, putting the drug on pace to meet its planned launch for the fourth quarter of 2017. Read More »

Imprimis Pharmaceuticals responds to FDA MedWatch notice

American Pharmacy News Reports | Aug 17, 2017
Imprimis has safely dispensed the referenced curcumin emulsion over 30,000 times without incident.

Imprimis Pharmaceuticals Inc. recently released a statement after the MedWatch notification put forth by the U.S. Food and Drug Administration. Read More »

GlobalMed unveils cutting-edge telemedicine platform

American Pharmacy News Reports | Aug 17, 2017
GlobalMed provides telemedicine hardware and software in 55 nations, last year logging over 3.5 million consultations.

Presenting a quantum leap in telemedicine, Scottsdale, Arizona-based GlobalMed recently released its award-winning branded eNcounter platform, designed to streamline clinical and at-home care and even geared for interoperability with wearable devices, ensuring data based outcomes. Read More »

FDA approves AbbVie's HCV infection drug Mavyret

American Pharmacy News Reports | Aug 17, 2017
AbbVie noted that around 3.4 million Americans are chronically infected with HCV.

AbbVie's once-daily treatment for chronic hepatitis C virus (HCV) infection, Mavyret, has been approved by the U.S. Food and Drug Administration. Read More »

La Jolla Pharmaceutical initiates EAP for investigation drug

American Pharmacy News Reports | Aug 17, 2017
The Food and Drug Administration facilitates EAPs to help expedite investigational medicines.

La Jolla Pharmaceutical Co. recently initiated an expanded access program (EAP) in the United States for its investigational drug LJPC-501. Read More »

FDA grants Breakthrough Therapy Designation to lymphoma drug

American Pharmacy News Reports | Aug 16, 2017
The designation will help expedite the development and regulatory review.

AstraZeneca and Acerta Pharma's treatment for patients with mantle cell lymphoma who have received at least one prior therapy was granted Breakthrough Therapy Designation by the U.S. Food and Drug Administration. Read More »

Pfizer's psoriatic arthritis treatment clears advisory committee

American Pharmacy News Reports | Aug 16, 2017
Psoriatic arthritis is a chronic, autoimmune, inflammatory disease.

Pfizer Inc.'s proposed dose of tofacitinib for the treatment of adult patients with active psoriatic arthritis received recommendation for approval by the U.S. Food and Drug Administration’s Arthritis Advisory Committee via a 10-1 vote. Read More »

CPPA awards accreditation to PANTHERx Specialty Pharmacy

American Pharmacy News Reports | Aug 16, 2017
Specialty pharmacies provide services that help patients achieve desired, cost-effective outcomes.

The Center for Pharmacy Practice Accreditation has awarded PANTHERx Specialty Pharmacy a practice accreditation. Read More »

FDA grants interim approval for Mylan’s TLD formulation

American Pharmacy News Reports | Aug 16, 2017
Mylan's TLD formulation is the first fixed-dose combination of its type to be distributed specifically for HIV/AIDS.

International pharmaceutical provider Mylan recently obtained what it called tentative approval of its New Drug Application for an antiretroviral formula to circulate as a preferred treatment for HIV/AIDS patients in developing nations. Read More »

NYU Langone Medical Center releases results from Alzheimer's study

American Pharmacy News Reports | Aug 16, 2017
Results of the trial were presented in London in July at the Alzheimer’s Association International Conference.

New York University Langone Medical Center has released results of an Alzheimer’s disease study that shows combining a specific care management program with commonly prescribed drugs multiplies the drug’s ability to improve daily function by roughly 7.5 times and stalls some of the disease’s effects. Read More »

Pharmacy association's executive director responds to DIR fee report

American Pharmacy News Reports | Aug 15, 2017
Sheila Arquette said the study is one of many in a long line paid for by pharmacy benefit managers.

National Association of Specialty Pharmacy Executive Director Sheila Arquette recently responded to a report on direct and indirect remuneration fees commissioned by the Pharmaceutical Care Management Association. Read More »

Moleculin Biotech comments on FDA approvals for AML drugs

American Pharmacy News Reports | Aug 15, 2017
Moleculin Biotech specializes in developing anti-cancer drug candidates.

Moleculin Biotech Inc. recently released comments regarding recent FDA approvals for new drugs that treat acute myeloid leukemia. Read More »

Radicava attains FDA approval for ALS treatment

American Pharmacy News Reports | Aug 15, 2017
Service care specialists are available to assist patients in finding the closest infusion facility.

Mitsubishi Tanabe Pharma America Inc. of New Jersey has reported that Radicava (edaravone), an intravenous therapy for adults with amyotrophic lateral sclerosis (ALS), is now available in the U.S. Read More »

Aimmune Therapeutics posits tentative peanut allergy answer

Carol Ostrow | Aug 15, 2017
t Aimmune’s investigational therapy targets an immune cell subset called TH2A cells — potentially desensitizing patients to the peanut allergy.

A trial treatment for peanut allergy has attracted attention in the media, with a recent Washington state publication highlighting California-based Aimmune Therapeutics Inc.’s “AR101” as a potential immunotherapy with the ability to impact allergen-specific T cells. Read More »

FDA approves Genentech’s Zelboraf for rare blood disease

American Pharmacy News Reports | Aug 15, 2017
Officials noted that the method is especially useful for work with rare diseases.

The U.S. Food and Drug Administration recently accepted Genentech’s supplemental New Drug Application for Zelboraf (vemurafenib) — including breakthrough therapy designation — to address a form of Erdheim-Chester disease, a rare blood disorder. Read More »

FDA approves Mavyret for hepatitis C virus

American Pharmacy News Reports | Aug 15, 2017
Previously, the course of hepatitis C virus therapy lasted at least 12 weeks.

The first eight-week medication cycle for chronic hepatitis C virus (HCV) recently earned approval from the U.S. Food and Drug Administration (FDA) in the form of Mavyret (glecaprevir and pibrentasvir), shortening treatment duration by one-third. Read More »

Impax Labs settles with parties on Opana ER rights

American Pharmacy News Reports | Aug 14, 2017
Impax Laboratories, Endo International and Penwest Pharmaceuticals recently revealed a mutual settlement agreement.

Resolving a contractual dispute dating to 2010 regarding three-way collaboration on Opana ER tablets — between Impax Laboratories, Endo International plc and Penwest Pharmaceuticals — Impax recently revealed a mutual settlement agreement from its Hayward, California hub. Read More »

Teva’s unique asthma inhaler gains FDA approval

American Pharmacy News Reports | Aug 14, 2017
Research has shown that approximately three-quarters of patients experience difficulty with MDI inhaler use.

An innovative new asthma treatment from Teva Pharmaceutical Industries Ltd. recently gained U.S. Food and Drug Administration approval, permitting the breath-activated inhaler to enter the market as a prophylactic maintenance medication. Read More »

CDC outlays over $200 million to curb contagious disease

Carol Ostrow | Aug 14, 2017
The 2017 investment will create a national laboratory for TB study.

Upping its game against certain candida, tuberculosis and gonorrhea strains, the U.S. Centers for Disease Control and Prevention recently allotted more than $200 million to help jurisdictions curtail both emerging and re-emerging infectious diseases. Read More »

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