Sun.Aug 27, 2023

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Old School Brand/Generic Crossword Puzzle

Med Ed 101

I know some folks out there really like crossword puzzles, so I figured why not combine a little fun with a little pharmacology education? I’ve created a free brand/generic crossword puzzle that you should be able to work through below. The main focus of this crossword puzzle is old school medications. The answers to the […] The post Old School Brand/Generic Crossword Puzzle appeared first on Med Ed 101.

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Selinexor by Karyopharm Therapeutics for Chronic Idiopathic Myelofibrosis (Primary Myelofibrosis): Likelihood of Approval

Pharmaceutical Technology

Selinexor is under clinical development by Karyopharm Therapeutics and currently in Phase II for Chronic Idiopathic Myelofibrosis (Primary Myelofibrosis).

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Trading Partners May Exhale: FDA Releases Guidance Exercising a Year-Long Period of Enforcement Discretion Related to DSCSA Enforcement of Certain Provisions

The FDA Law Blog

By Karla L. Palmer — On Friday, August 25, 2023, FDA released a much-anticipated Final Guidance titled, “Enhanced Drug Distribution Security Requirements Under Section 582(g)(1) of the Federal Food, Drug, and Cosmetic Act,” addressing FDA’s implementation of certain electronic interoperability provisions of the Drug Supply Chain Security Act (DSCSA), which were due to become effective on November 27, 2023.

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Risk adjusted net present value: What is the current valuation of Sarepta Therapeutics’s Patidistrogene bexoparvovec?

Pharmaceutical Technology

Patidistrogene bexoparvovec is a gene therapy commercialized by Sarepta Therapeutics, with a leading Phase II program in Limb-Girdle Muscular Dystrophy.

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Position Your Pharmacy for Expansion

Speaker: Chris Antypas and Josh Halladay

Access to limited distribution drugs and payer contracts are key to pharmacy expansion. But how do you prepare your operations to take the next step? Meaningful data: Collect and share clinical data regarding outcomes, utilization, and more Reporting: Limited distribution models require efficient tracking and reporting systems Workflows: Align workflows with specific pharma and payer contractual requirements For in-depth, expert insights on pharmacy expansion, watch this webinar from Inovalon.

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NCPA applauds one-year delay of FDA enforcement of DSCSA interoperability provisions

Drug Store News

The one-year delay allows for smoother implementation and a better patient experience, NCPA said.

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Selinexor by Karyopharm Therapeutics for Chronic Idiopathic Myelofibrosis (Primary Myelofibrosis): Likelihood of Approval

Pharmaceutical Technology

Selinexor is under clinical development by Karyopharm Therapeutics and currently in Phase II for Chronic Idiopathic Myelofibrosis (Primary Myelofibrosis).

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Signal: Allina health will no longer bar indebted patients from care

Pharmaceutical Technology

Following public outcry and a government investigation, Allina Health has reneged on their policy barring debtors from out-patient care.

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Himalaya Wellness unveils Ashwagandha Organic Gummies

Drug Store News

Himalaya Wellness is introducing blackberry-flavored, vegan Ashwagandha Organic Gummies.

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BR-6002 by Boryung Pharmaceutical for Cardiovascular Disease: Likelihood of Approval

Pharmaceutical Technology

BR-6002 is under clinical development by Boryung Pharmaceutical and currently in Phase I for Cardiovascular Disease.

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Himalaya Wellness unveils Ahwagandha Organic Gummies

Drug Store News

Himalaya Wellness is introducing blackberry-flavored, vegan Ashwagandha Organic Gummies.

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What the FDA's New Dosage Guidance Means for the Future of Clinical Research

Speaker: Dr. Ben Locwin - Biopharmaceutical Executive & Healthcare Futurist

What will the future hold for clinical research? A recent draft from the FDA provides valuable insight. In "Optimizing the Dosage of Human Prescription Drugs and Biological Products for the Treatment of Oncologic Diseases," the FDA notes that "targeted therapies demonstrate different dose-response relationships compared to cytotoxic chemotherapy, such that doses below the Maximum Tolerated Dose (MTD) may have similar efficacy to the MTD but with fewer toxicities.

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BR-6002 by Boryung Pharmaceutical for Cardiovascular Disease: Likelihood of Approval

Pharmaceutical Technology

BR-6002 is under clinical development by Boryung Pharmaceutical and currently in Phase I for Cardiovascular Disease.

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St. Ives debuts new exfoliating toners

Drug Store News

Apricot, Rose and Unfragranced are the three new exfoliating toners offered by St. Ives.

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Safinamide mesylate by Zambon Co for Multiple System Atrophy (MSA or Shy-Drager Syndrome or Multi-System Degeneration): Likelihood of Approval

Pharmaceutical Technology

Safinamide mesylate is under clinical development by Zambon Co and currently in Phase II for Multiple System Atrophy (MSA or Shy-Drager Syndrome or Multi-System Degeneration).

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Safinamide mesylate by Zambon Co for Multiple System Atrophy (MSA or Shy-Drager Syndrome or Multi-System Degeneration): Likelihood of Approval

Pharmaceutical Technology

Safinamide mesylate is under clinical development by Zambon Co and currently in Phase II for Multiple System Atrophy (MSA or Shy-Drager Syndrome or Multi-System Degeneration).

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5 Reasons to Upgrade Your Pharmacy Management Software

Are you still using workarounds to manage your daily operations? To achieve peak performance, it's time to explore other options for specialty and infusion pharmacy software. Streamline pharmacy operations and improve clinical performance with automated processing, real-time data exchange, and electronic decision support. Download this helpful infographic to: Drive efficiency and patient adherence from referral receipt to delivery and ongoing care – all with our Pharmacy Cloud.

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Risk adjusted net present value: What is the current valuation of Jazz Pharmaceuticals’s Zanidatamab?

Pharmaceutical Technology

Zanidatamab is a monoclonal antibody commercialized by Jazz Pharmaceuticals, with a leading Phase III program in Adenocarcinoma Of The Gastroesophageal Junction.

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Risk adjusted net present value: What is the current valuation of Avalo Therapeutics’s Quisovalimab?

Pharmaceutical Technology

Quisovalimab is a monoclonal antibody commercialized by Avalo Therapeutics, with a leading Phase II program in Crohn's Disease (Regional Enteritis).

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Lutetium (lu177) lilotomab satetraxetan by Thor Medical for B-Cell Chronic Lymphocytic Leukemia: Likelihood of Approval

Pharmaceutical Technology

Lutetium (lu177) lilotomab satetraxetan is under clinical development by Thor Medical and currently in Phase II for B-Cell Chronic Lymphocytic Leukemia.

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Lutetium (lu177) lilotomab satetraxetan by Thor Medical for B-Cell Chronic Lymphocytic Leukemia: Likelihood of Approval

Pharmaceutical Technology

Lutetium (lu177) lilotomab satetraxetan is under clinical development by Thor Medical and currently in Phase II for B-Cell Chronic Lymphocytic Leukemia.

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Risk adjusted net present value: What is the current valuation of Scholar Rock Holding’s Linavonkibart?

Pharmaceutical Technology

Linavonkibart is a monoclonal antibody commercialized by Scholar Rock Holding, with a leading Phase I program in Non-Small Cell Lung Cancer.

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BR-6002 by Boryung Pharmaceutical for Duodenal Ulcer: Likelihood of Approval

Pharmaceutical Technology

BR-6002 is under clinical development by Boryung Pharmaceutical and currently in Phase I for Duodenal Ulcer.

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BR-6002 by Boryung Pharmaceutical for Gastric Ulcers: Likelihood of Approval

Pharmaceutical Technology

BR-6002 is under clinical development by Boryung Pharmaceutical and currently in Phase I for Gastric Ulcers.

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BR-6002 by Boryung Pharmaceutical for Duodenal Ulcer: Likelihood of Approval

Pharmaceutical Technology

BR-6002 is under clinical development by Boryung Pharmaceutical and currently in Phase I for Duodenal Ulcer.

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BR-6002 by Boryung Pharmaceutical for Gastric Ulcers: Likelihood of Approval

Pharmaceutical Technology

BR-6002 is under clinical development by Boryung Pharmaceutical and currently in Phase I for Gastric Ulcers.

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