Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
ADD008 is a proprietary, sulfite-free, and heat-stable aqueous formulation of adrenaline (epinephrine) developed by Theravia for the emergency treatment of anaphylaxis. Conventional adrenaline formulations, such as those used in EpiPen, typically require sulfite preservatives (e.g., sodium metabisulfite) to prevent oxidation; however, these sulfites can trigger hypersensitivity reactions in some patients and limit the product's stability at higher temperatures. ADD008 utilizes a novel stabilization technology to provide a sulfite-free alternative that is designed for intramuscular delivery via standard, off-the-shelf auto-injectors. The program is currently in Phase 1 clinical development (NCT05843123), with studies evaluating its pharmacokinetic and pharmacodynamic profile in comparison to established adrenaline auto-injectors like EpiPen and Anapen.
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 ADD008.