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Pedmark STS

Phase 2

Solid Tumor Malignancies | Small molecule | Oncology |Fennec Pharmaceuticals Inc.|Last Updated: Feb 12, 2026

Success Probability
Approval Probability 71%
TA Base Rate26%
Adjusted LOA41%
ML RiskLOW_RISK
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Market & Valuation
rNPV $3.2B
Market Size $9.4B
Revenue Basis $1.6B
Competitors 6
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Trial Design
UNCONTROLLED
Total Trials1
Total Enrollment25
FDA Designations
ORPHAN_DRUG
Clinical Trials (1)
NCT IDTitlePhaseStatusEnrollmentVelocityDesignStartCompletionLast UpdatedSitesCountries
NCT07407582Ph. I/II Sodium Thiosulfate for OtoProtection During Cisplatin (STOP-CIS)PHASE2 NOT YET_RECRUITING 25Apr 30, 2026Apr 30, 2028Feb 12, 20261 United States
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Study Design & Arms
AllocationNA
MaskingNONE
PurposeTREATMENT
Interventions
NameTypeDescription
Pedmark® STSDRUGPedmark® STS (20 g/m2) will be given via intravenous infusion over 15-30 minutes, starting 6 hours after the completion of cisplatin infusion. Pedmark® STS will be given each day of cisplatin infusion.
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Recent Changes (Last 90 Days)
LOWMay 24, 2026NCT07407582studyFirstPostDate: changed