Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
HAL-MRE1 is a subcutaneous allergen immunotherapy being developed by HAL Allergy Group for the treatment of ragweed-induced allergic conditions. It is formulated as a liquid suspension containing modified allergens extracted from ragweed pollen adsorbed onto aluminum hydroxide. [6] As an allergen immunotherapy, it aims to modify the underlying cause of the allergy by administering controlled doses of the allergen, which helps the immune system to build tolerance and reduce the allergic response. [2] A first-in-human, Phase 1 clinical trial (NCT03758456) was initiated to evaluate its safety and tolerability in adults with ragweed-induced allergic rhinitis or rhinoconjunctivitis, with or without asthma. [6]
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 hal-mre1.