Ofirnoflast - Halia Therapeutics
Alternative Names: HT 6184Latest Information Update: 11 Aug 2026
At a glance
- Originator Halia Therapeutics
- Class Amides; Amines; Analgesics; Aniline compounds; Anti-inflammatories; Antianaemics; Antidementias; Antineoplastics; Cyclopropanes; Eye disorder therapies; Fluorinated hydrocarbons; Fluorobenzenes; Isoxazoles; Obesity therapies; Pyrimidines; Pyrroles; Small molecules; Urea compounds
- Mechanism of Action NEK7 protein inhibitors; NLRP3 protein inhibitors
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Orphan Drug Status
Yes - Myelodysplastic syndromes
Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.
- New Molecular Entity Yes
Highest Development Phases
- Phase II Inflammatory pain; Myelodysplastic syndromes; Obesity
- Preclinical Acute myeloid leukaemia; Eye disorders; Haemolytic anaemia
- Research Alzheimer's disease
- No development reported Inflammation
Most Recent Events
- 31 Jul 2026 Halia Therapeutics plans a phase-II trial for Myelodysplastic syndromes (Treatment-experienced) in October 2026 (PO) (NCT07738510)
- 15 Jun 2026 Ofirnoflast receives Fast Track designation for Myelodysplastic syndromes [PO] in USA
- 12 May 2026 Efficacy and adverse events data from a phase IIa trial in Myelodysplastic syndromes released by Halia Therapeutics