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Gilead wins patent battle with US government over HIV PrEP drugs

Pharmaceutical Technology

According to the US government, Gilead had repeatedly refused to license patents related to PrEP research undertaken by the Department of Health and Human Services’ (HHS) Centers for Disease Control and Prevention (CDC). While both Descovy and Truvada contain emtricitabine, they feature different forms of the antiviral tenofovir.

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Soliton Appoints Sean J. Shapiro as Vice President of Sales

The Pharma Data

Shapiro as Vice President of Sales, effective January 1, 2021. Sean is a seasoned sales executive who has successfully launched several aesthetic devices in the industry, and we look forward to leveraging his extensive experience as we prepare for the commercial launch of our RAP technology during the first half of next year.”

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CSL doses first patient with haemophilia B gene therapy Hemgenix

Pharmaceutical Technology

Hemgenix works by dosing a patient with an engineered adeno-associated virus (AAV), containing the gene responsible for producing a protein called factor IX. Already a big player in haemophilia treatments, CSL licensed exclusive global rights to Hemgenix from gene therapy developers uniQure back in 2021.

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Biopharma Packaging Requirements: What You Need to Know

Pharma Packaging Solutions

Licensing: The CFR states that all packaging and labeling must be performed in a properly licensed facility. Final Container Label, Carton Label, and Enclosure Regulations (From Section 112.2) Here is a brief overview of biologics packaging and labeling requirements according to the Code of Federal Regulations.

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Bang Energy’s Twist of Fate: Monster Energy as Potential Buyer

XTalks

This transaction is pending approval from the bankruptcy court and the Federal Trade Commission (FTC), which is currently reviewing the potential sale; however, if given the green light, this deal could potentially be beneficial for both brands. billion in sales, closely followed by Monster with $4.9 billion, according to Statista.

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Relay Therapeutics Announces a Worldwide License and Collaboration Agreement with Genentech for RLY-1971

The Pharma Data

. Relay Therapeutics will receive $75 million upfront and is eligible to receive an additional $25 million in near-term payments and $695 million in additional potential milestones, plus royalties on global net product sales. sales and up to $410 million in additional ex-U.S. CAMBRIDGE, Mass., About RLY-1971.

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Radioligand therapy pipeline with in-license for compounds targeting Fibroblast Activation Protein (FAP)

The Pharma Data

This press release contains forward-looking statements within the meaning of the United States Private Securities Litigation Reform Act of 1995. These targeted drugs bind to markers or proteins over-expressed by certain tumors, or tumor-associated tissue, such as stroma. Disclaimer. Source link:[link].

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