Study of PBI-200 in Subjects With NTRK-Fusion-Positive Solid Tumors (NCT04901806) | Clinical Trial Compass
TerminatedPhase 1
Study of PBI-200 in Subjects With NTRK-Fusion-Positive Solid Tumors
Stopped: Sponsor terminated development of PBI-200
United States29 participantsStarted 2021-07-20
Plain-language summary
This is a first-in-human, open-label, multicenter, dose-escalation, safety, PK, and biomarker study of PBI-200 in subjects with NTRK-fusion-positive advanced or metastatic solid tumors.
Who can participate
Age range18 Years
SexALL
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Key Inclusion Criteria:
* Subject has one of the following solid tumors which has progressed on or following at least one systemic therapy regimen administered for advanced or metastatic disease or for which no approved therapy exists:
* NTRK-fusion-positive, locally advanced (i.e., not amenable to surgical resection) or metastatic solid tumor Note: Subjects with any grade of malignant glioma previously treated with systemic therapy are eligible.
Phase 1
* NTRK-gene amplified, locally advanced or metastatic solid tumor
* EWSR1-WT1-positive DSRCTs.
* Subjects with NTRK-fusion-positive solid tumors other than primary brain tumors must have previously received treatment with a TRK inhibitor, unless the subject does not have access to TRK-inhibitor therapy (e.g., no TRK inhibitor is marketed and available to the subject in the subject's country) or the subject has declined treatment with available marketed TRK inhibitors.
* Subjects with NTRK-gene amplified solid tumors, primary brain tumors or EWSR1-WT1-positive DSRCTs may have received prior treatment with a TRK inhibitor but this is not required.
Phase 2
* Has measurable disease by RECIST v1.1 for subjects with non-brain primary tumors or RANO criteria for subjects with primary brain tumors.
* Subjects with non-brain primary tumors must have previously received treatment with a TRK inhibitor and a documented resistance mutation(s) (e.g., solvent front, gatekeeper or xDFG mutation). Archival tissue from a prior biopsy t…
What they're measuring
1
Phase 1: Number of patients with AEs
Timeframe: Through study completion, estimated as an average of 36 months
2
Phase 1: Recommended Phase 2 Dose
Timeframe: Approximately 12 months
3
Phase 2: Cohort A - Overall Response Rate (ORR)
Timeframe: Through study completion, estimated as an average of 36 months
4
Phase 2: Cohort B - ORR
Timeframe: Through study completion, estimated as an average of 36 months