Drug

Doxribtimine

As of the edition of 20 October 2026, Doxribtimine is a small molecule: marketed, first approved in 2025 (US); no US protection is listed.

Sources: FDA Orange Book and Purple Book, other approval registers, ClinicalTrials.gov, ChEMBL.

The drug

Status
Marketed; latest approval 2026
Kind
Small molecule
Brand name
Kygevvi
First approved
3 November 2025 (US)
Approvals on record
2 in 2 regions
Holder of the most recent approval
UCB; 2 holders in all
Registered trials
8, 1 stopped early
Disease areas
Bones, joints and muscles; Nervous system; Nutrition and metabolism; Inherited and neonatal; Blood and lymph; Digestive system

US protection

No US protection is listed.

The FDA registers list no drug-substance patent or exclusivity that counts for this drug.

This is the US only.

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated2100
Phase 11010
Phase 24220
Phase 31001
All trials8

Who has held its approvals

CompanyRoleYears
UCBOriginator and Lead sponsor of trials2026 to now