Peripheral T-Cell Lymphoma, Not Otherwise Specified · registered primary completion 2027-11-01 · NCT06561048
No approved product carries Peripheral T-Cell Lymphoma, Not Otherwise Specified on label.
Registered design for NCT06561048: randomized, open-label, 150 participants (estimated). Primary outcome: Progression-free survival.
Cash of $215M against operating outflow of $14M per quarter gives roughly 15.7 quarters of runway, clearing the registered primary completion 4.7 quarters out by 11.0 quarters.
84,120,944 shares outstanding against 98,149,121 if every outstanding option, warrant and convertible were exercised. In that case 14.3% of a gain in enterprise value would accrue to those holders rather than to current shareholders.
Designations disclosed: Breakthrough Therapy, Fast Track, Orphan Drug, PRIME (EU). These accelerate review and, for Orphan, confer exclusivity if approved; none is evidence of efficacy.
4 distinct molecules in 3 active company-sponsored trials; Soquelitinib accounts for 2 of them at Phase 2/Phase 3.