Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Zinc diethylenetriaminepentaacetic acid (Zn-DTPA) is a small molecule chelating agent indicated for the treatment of individuals with known or suspected internal contamination with transuranic radioactive elements, specifically plutonium, americium, or curium. By forming stable, water-soluble complexes with these metal ions, Zn-DTPA facilitates their elimination from the body through renal excretion, thereby reducing the internal radiation dose. Approved by the U.S. FDA in 2004, it is administered either by intravenous injection or by nebulizer for inhalation contamination. Zn-DTPA is particularly preferred for maintenance therapy or when treatment begins more than 24 hours after contamination, as it is less likely than calcium-DTPA to deplete essential endogenous trace metals such as zinc and manganese.
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 zinc diethylenetriaminepentaacetic acid.