Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Chamomilla recutita topical formulation refers to a series of botanical preparations, including a 8.35% gel and a 2.5% infusion, developed by the University of Brasilia for the management of radiodermatitis. The drug utilizes the therapeutic properties of German chamomile, which contains active compounds like alpha-bisabolol and chamazulene known for their potent anti-inflammatory, antioxidant, and wound-healing effects. By inhibiting the inflammatory cascade and neutralizing reactive oxygen species generated during radiotherapy, these formulations aim to prevent and treat skin damage in patients undergoing treatment for breast or head and neck cancers. The development program includes a Phase 3 clinical trial (NCT02251392) comparing the efficacy of these chamomile-based interventions against standard urea-based creams.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on chamomilla recutita topical formulation.