A Phase 1 interventional study of PBI-200 in Solid Tumor, Adult, Brain Tumor, Primary and Desmoplastic Small Round Cell Tumor, sponsored by Pyramid Biosciences. Terminated at 42 sites in 11 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-03-28.
Sponsored by Pyramid Biosciences · Phase 1, Interventional, and Treatment
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.
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. Phase 1 will also include subjects with NTRK-amplified advanced or metastatic solid tumors or refractory EWSR1-WT1-fusion-positive desmoplastic small round cell tumors (DSRCTs).
Phase 1 is the dose-escalation portion of the study in which the evaluation of safety and tolerability and establishing the RP2D are primary objectives. Once the RP2D has been established, two expansion cohorts will open to accrual, a Non-Brain Primary Tumor cohort and a Primary Brian Tumor cohort.
Although this was intended to be a Phase 1/2 trial, the trial was terminated without proceeding to Phase 2.
9,365 studies on the registry are indexed under Neoplasms; 2,489 are open to participants now.
This study's enrollment of 29 is below the median of 50 across 7,253 interventional studies indexed under Neoplasms.
Browse Neoplasms studies →Pyramid Biosciences is the lead sponsor of 7 studies on the registry; none are open to participants now.
Of its 7 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.
Counted across the registry records on this site, refreshed daily.
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:
Phase 1
Phase 2
Key Exclusion Criteria:
Cytotoxic chemotherapy, biologic agent, investigational agent, or radiation therapy ≤ 3 weeks prior to the first dose of PBI-200 (6 weeks for nitrosoureas).
Drug: PBI-200
Drug: PBI-200
PBI-200 will be administered orally over continuous 28-day cycles
Phase 1: Number of patients with AEs
Severity of AEs will be assessed according to the NCI CTCAE v5.0
Time frame: Through study completion, estimated as an average of 36 months
Phase 1: Recommended Phase 2 Dose
Time frame: Approximately 12 months
Phase 2: Cohort A - Overall Response Rate (ORR)
Assessed using Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1
Time frame: Through study completion, estimated as an average of 36 months
Phase 2: Cohort B - ORR
Assessed using Response Assessment in Neuro-Oncology (RANO) criteria
Time frame: Through study completion, estimated as an average of 36 months
Phase 1: Area under the plasma drug concentration-time curve from 0 to 24 hours after one dose and after 28 doses
Time frame: 29 days
Phase 1: ORR
Assessed by RECIST for subjects with non-brain primary tumors and by RANO for subjects with primary brain tumors
Time frame: Through study completion, estimated as an average of 36 months
Duration of Response (DoR)
Assessed by RECIST for subjects with non-brain primary tumors and by RANO for subjects with primary brain tumors
Time frame: Through study completion, estimated as an average of 36 months
Progression-free Survival
Assessed by RECIST for subjects with non-brain primary tumors and by RANO for subjects with primary brain tumors
Time frame: Through study completion, estimated as an average of 36 months
Plan to share: No
No publications or documents are linked to this record.
This study is terminated, as verified in Mar 2024. You cannot join it, but the record below documents what was studied.
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Pyramid Biosciences