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Pharmanovia taps Nanoform to improve bioavailability of ‘iconic branded medicine’

Outsourcing Pharma

The pharmaceutical company has forged a partnership with the nanotechnology specialist to use nanoparticle tech and formulation to advance its products.

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Positive Phase I results for solid dose prescription CBD medicine

Drug Discovery World

Positive Phase I results for a new solid dose prescription cannabidiol (CBD) demonstrate the tolerability and bioavailability of the drug. The post Positive Phase I results for solid dose prescription CBD medicine appeared first on Drug Discovery World (DDW).

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Sponsored: Jubilant’s Precision Medicines Offer Safety, Therapeutic Advantages in Cancer, Immunol.

BioSpace

Jubilant Therapeutics's differentiated, orally bioavailable molecules address both validated and novel therapeutic targets in oncology and immunology.

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FDA expands organ-on-a-chip research collaboration

Drug Discovery World

The system will initially be investigated for improving the preclinical estimation of human drug bioavailability compared to standard animal models. . Bioavailability is defined as the fraction of drug reaching the bloodstream. Changes to rules for animal testing .

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PureTech Reveals New CBD Pill to Rival Jazz’s Epidiolex

XTalks

Clinical-stage biotech company PureTech Health has announced it has developed a new oral CBD therapeutic candidate with improved bioavailability and tolerability, which could expand use of the CBD prodrug in a wide range of indications and age groups. Jazz bought out Epidiolex developer GW Pharmaceuticals for the drug in a whopping $7.2

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Scilex buys rights to acute migraine treatment Elyxyb in Canada and the US

Pharmaceutical Technology

It is formulated using a self-micro-emulsifying drug delivery system that improves the drug’s bioavailability and solubility. Scilex stated that the unit dose of Elyxyb oral solution makes it convenient for people to take medicine immediately during acute migraine attacks.

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BeiGene’s Brukinsa receives UK marketing authorisations to treat cancers

Pharmaceutical Technology

BeiGene has received marketing authorisations for Brukinsa (zanubrutinib) in Great Britain from the Medicines and Healthcare products Regulatory Agency (MHRA) to treat chronic lymphocytic leukemia (CLL) and marginal zone lymphoma (MZL).

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