INNOVATION
With continuous innovation as a key driver for our sustainable growth, our R&D teams work relentlessly to help ensure we meet individual consumer and patient needs with superior outcomes. We have developed a best-in-class pipeline and a track record of first-to-market innovation.
We aim to become the leader in dermatology, prioritizing biotechnologies for injectable and oral products. A top priority for us is the development of the investigational therapy nemolizumab for atopic dermatitis, prurigo nodularis and chronic kidney disease-associated pruritus. We are actively investigating other indications within and beyond dermatology.
OUR POLICY ON EXPANDED ACCESS PROGRAM
Galderma believes clinical trials are the most appropriate way for patients to access investigational medicines developed by Galderma. In these trials, the safety and efficacy of investigational medicines are rigorously assessed by Galderma and the relevant regulatory agencies in order to understand the medicine’s benefits, risks, and appropriate use, including whether or not it should be approved as a therapy for its intended use. Obtaining regulatory approval is the best way to bring safe and effective medicines to the greatest number of patients who may benefit from treatment.
At this time, Galderma does not have an expanded access program that allows patients to have access to the company’s investigational therapies outside of clinical trials or prior to FDA approval. Galderma may update this policy as drug development programs are progressing and reassess the approach to expanded access programs. Should patients, families, or physicians have any questions, please contact our Medical Information department by email via the contact us form.
