Remove topic excipients
article thumbnail

Drug Digest: The Shape of Things to Come: Advances and Improvements in Excipients

PharmaTech

In this episode of Drug Digest, Pharmaceutical Technology’s European/Senior Editor, Felicity Thomas, chats about the biggest trends impacting oral and topical drug delivery and how these trends are impacting the excipient sector with Nick DiFranco and Ashley Rezak from Lubrizol Life Science Health.

article thumbnail

Enhancing bioavailability in ocular drug delivery

European Pharmaceutical Review

Currently, effective topical administration is challenging as the industry aims to prolong drug residence time and guarantee appropriate ocular permeation. How to enhance ocular drug bioavailability One approach to enhance drug bioavailability after topical administration is increasing corneal permeability.

Insiders

Sign Up for our Newsletter

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

Trending Sources

article thumbnail

Krystal Biotech receives FDA approval for DEB topical gene therapy

Pharmaceutical Technology

Krystal Biotech has received approval from the US Food and Drug Administration for topical gene therapy VYJUVEK to treat dystrophic epidermolysis bullosa (DEB) in adults and in children aged six months and above. Topic sponsors are not involved in the creation of editorial content.

article thumbnail

Novaliq’s dry eye disease therapy receives US FDA approval

Pharmaceutical Technology

VEVYE, the development name of which is CyclASol, is a cyclosporine, solubilised solution in a new, water-free excipient. CyclASol is topical anti-inflammatory and immunomodulating ophthalmic drug solution containing 0.1%

article thumbnail

Roquette opens pharmaceutical innovation facility in Pennsylvania, US

Pharmaceutical Technology

In the first phase of its training workshops, the Pharmaceutical Innovation Center plans to develop a range of excipients [inactive substances that serve as the vehicle or medium for a drug or other active substance] for controlled release dosage forms, improving their bioavailability, along with formulating orally dispersible and chewable tablets.

article thumbnail

RT-002 by Revance Therapeutics for Upper Limb Muscle Spasticity: Likelihood of Approval

Pharmaceutical Technology

It is investigating its lead candidate, daxibotulinumtoxinA, a topical gel formulation as a needle-free approach for a wide range of therapeutic and aesthetic indications, such as chronic migraine, facial wrinkles and muscle disorders. Revance Therapeutics is headquartered in Nashville, Tennessee, the US.

article thumbnail

RT-002 by Revance Therapeutics for Upper Limb Muscle Spasticity: Likelihood of Approval

Pharmaceutical Technology

It is investigating its lead candidate, daxibotulinumtoxinA, a topical gel formulation as a needle-free approach for a wide range of therapeutic and aesthetic indications, such as chronic migraine, facial wrinkles and muscle disorders. Revance Therapeutics is headquartered in Nashville, Tennessee, the US.