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OncoMatch/Clinical Trials/NCT04196257

BP1001-A in Patients With Advanced or Recurrent Solid Tumors

Is NCT04196257 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1 trial studies multiple treatments including BP1001-A (Liposomal Grb2 Antisense Oligonucleotide) and BP1001-A (Liposomal Grb2 Antisense Oligonucleotide) with paclitaxel for solid tumor, adult.

Phase 1RecruitingBio-Path Holdings, Inc.NCT04196257Data as of Jun 2026

Treatment: BP1001-A (Liposomal Grb2 Antisense Oligonucleotide) · BP1001-A (Liposomal Grb2 Antisense Oligonucleotide) with paclitaxelThis is a phase I, open-label, study of BP1001-A in participants with advanced or recurrent solid tumors. The dose escalation phase will determine the safety and the maximum tolerated dose (MTD) or maximum administered dose (MAD) of BP1001-A as a single agent. After the MTD or MAD of BP1001-A is established, the dose expansion phase will commence and determine the safety, toxicity and response of BP1001-A in combination with paclitaxel.

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Extracted eligibility criteria

Treatments studied

Chemotherapy

BP1001-A (Liposomal Grb2 Antisense Oligonucleotide) with paclitaxel

Other

BP1001-A (Liposomal Grb2 Antisense Oligonucleotide)

Cancer type

Tumor Agnostic

Ovarian Cancer

Endometrial Cancer

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Cannot have received: bone marrow or hematopoietic stem cell transplant

Participants who had previous bone marrow or hematopoietic stem cell transplant

Lab requirements

Blood counts

HgB ≥ 9 g/dL, WBC ≥ 3,000/mcL, ANC ≥ 1,500/mcL, PLT ≥ 100,000/mcL

Kidney function

Serum creatinine < 1.5 x ULN or eGFR > 60 mL/min according to Cockcroft-Gault formula

Liver function

Total bilirubin within normal institutional limits, AST and ALT < 2.5 X institutional ULN

Participants must have adequate: Bone marrow function: HgB ≥ 9 g/dL, WBC ≥ 3,000/mcL, ANC ≥ 1,500/mcL, PLT ≥ 100,000/mcL; Hepatic function: Total bilirubin within normal institutional limits, AST and ALT < 2.5 X institutional ULN; Renal function: Serum creatinine < 1.5 x ULN or eGFR > 60 mL/min according to Cockcroft-Gault formula

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Holy Cross Hospital · Silver Spring, Maryland
  • Karmanos Cancer Institute · Detroit, Michigan
  • Mary Crowley Cancer Research · Dallas, Texas
  • The University of Texas M.D. Anderson Cancer Center · Houston, Texas

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT04196257 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior bone marrow or hematopoietic stem cell transplant disqualifies patients from enrollment.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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