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Clinical trial

A Phase I/IIa, Dose Escalation Study Evaluating the Safety, Tolerability, and Preliminary Efficacy of Intraductal Administration of RXRG001 to Parotid Gland(s) in Adults With Radiation-Induced Xerostomia and Hyposalivation

NCT06714253 is registered in ClinicalTrials.gov with RiboX Therapeutics Ltd. as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase I/IIa, Dose Escalation Study Evaluating the Safety, Tolerability, and Preliminary Efficacy of Intraductal Administration of RXRG001 to Parotid Gland(s) in Adults With Radiation-Induced Xerostomia and Hyposalivation
Lead sponsor
RiboX Therapeutics Ltd.
Phase
Phase 1/2
Overall status
Recruiting
Start date
March 5, 2025
Completion date
August 31, 2027
Enrollment
42 (estimated)
Sites
5

Conditions

As the registry lists them; a condition with its own page is linked.

radiation-induced xerostomia and hyposalivation