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PH-762

Phase 1

Squamous Cell Carcinoma of the Skin | Small molecule | Oncology |Phio Pharmaceuticals Corp.|Last Updated: Feb 11, 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
UNCONTROLLEDDMCBiomarker
Total Trials1
Total Enrollment30
FDA Designations
No designations recorded
Clinical Trials (1)
NCT IDTitlePhaseStatusEnrollmentVelocityDesignStartCompletionLast UpdatedSitesCountries
NCT06014086Intratumoral PH-762 for Cutaneous CarcinomaPHASE1 ACTIVE NOT_RECRUITING 30Nov 7, 2023Mar 1, 2026Feb 11, 20265 United States
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Study Endpoints
Primary Endpoints
Adverse Events
16 weeks

Incidence, severity, seriousness and relatedness of all treatment-emergent adverse events.

Secondary Endpoints
Pharmacokinetics: maximum plasma concentration (Cmax)
3.5 weeks
Pharmacokinetics: time to maximum plasma concentration (Tmax)
3.5 weeks
Pharmacokinetics: area under the curve to last quantifiable plasma concentration (AUClast)
3.5 weeks
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Study Design & Arms
AllocationNA
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT
Treatment Arms
ArmTypeDescription
Sequential escalating doses of PH-762.EXPERIMENTALEscalating doses of PH-762 are to be tested, with an observation period between doses.
Interventions
NameTypeDescription
PH-762DRUGPH-762 is a potent RNAi molecule targeting PD-1.
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Eligibility Criteria
Age Range18 Years — N/A
SexALL
Healthy VolunteersNo
Study Sites5

Key Inclusion Criteria: * Histologically confirmed cutaneous squamous cell carcinoma (cSCC), melanoma, or Merkel cell carcinoma, meeting one of the following criteria: * cSCC, resectable local tumors: must be Stage II or lower, amenable to curative resection and in a location where acceptable su...

Countries:United States
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Recent Changes (Last 90 Days)
LOWMay 26, 2026NCT06014086primaryCompletionDate: changed
LOWMay 24, 2026NCT06014086studyFirstPostDate: changed