Clinical Trial 23071

• Overview

  Study Title:

  A Phase 1, Open-label Study of Oral BDTX-4933 in Patients with KRAS, BRAF and Other Select RAS/MAPK Mutation Positive Neoplasms

  Summary:

  Phase 1 dose escalation and an expansion cohort study designed to evaluate the safety and tolerability, maximum tolerated dose (MTD) and the preliminary recommended Phase 2 dose (RP2D), and antitumor activity of BDTX-4933.

  Objective:

  Primary: * To determine the MTD, if one exists, and the preliminary RP2D of BDTX-4933 Secondary: * To evaluate the safety and tolerability of BDTX-4933 * To characterize the plasma PK profile of BDTX-4933 and its metabolite BDTX-7037 * To evaluate preliminary antitumor activity of BDTX-4933 * To evaluate the OS of BDTX-4933 compared to historical control

• Treatments

  Therapies:

  Therapy (NOS)

  Medications:

  BDTX-4933 ()

• Inclusion Criteria

  Inclusion Criteria: Disease criteria:
  • Histologically or cytologically confirmed recurrent/advanced (unresectable) or metastatic solid tumors or histiocytic neoplasms with documented RAS or BRAF mutations. Note: Patients may have stable central nervous system (CNS) metastases. Patients with active CNS metastases or primary CNS tumors associated with progressive neurological symptoms or needing increased doses of corticosteroids to control the CNS disease are excluded from the study. Dose Escalation cohorts:
  • NSCLC with KRAS non-G12C mutations, including other mutations at KRAS-G12 (eg, G12V/G12D) and other oncogenic variants of KRAS mutations on G13 and Q61 amino acid residues, BRAF, or CRAF mutations.
  • Melanoma with BRAF, CRAF, or NRAS mutations.
  • Histiocytic neoplasms with BRAF or NRAS mutations.
  • Thyroid carcinoma with BRAF mutations.
  • Colorectal carcinoma with BRAF (Class II or III) mutations with Sponsor approval.
  • Other solid tumors with BRAF Class I mutations after prior treatment with a BRAF/MEK inhibitor or local standard-of-care with Sponsor approval. Dose Expansion cohort:
  • Recurrent advanced/metastatic NSCLC with KRAS non-G12C mutations without small cell lung cancer transformation with progressive disease confirmed by radiographic assessment. Prior standard-of-care For dose levels > Exhausted all available standard-of-care therapies or, in the opinion of the Investigator, would be unlikely to tolerate or derive clinically meaningful benefit from available standard-of-care therapy.
  • Patients with eligible tumors harboring BRAF V600E mutations must have received FDA approved BRAF targeted therapy, BRAF/MEK inhibitors combination, or BRAF inhibitors combination. For dose levels 200 mg or more once daily or at preliminary RP2D(s):
  • Patients must have received at least 1 but no more than 2 prior lines of systemic therapy for metastatic/advanced disease (adjuvant and maintenance therapy do not count towards the limit).
  • Evaluable or measurable disease in dose escalation and measurable disease only for dose expansion cohorts.
  • Adequate bone marrow and organ function.
  • Recovered from toxicity to prior anti-cancer therapy.
  • Appropriate candidate for BDTX-4933 monotherapy.
  • Life expectancy of >=12 weeks in the opinion of the Investigator.

• Exclusion Criteria

  Exclusion Criteria:
  • Cancer that has a known MEK1/2 mutation.
  • Major surgery within 4 weeks of study entry or planned during study.
  • Ongoing anticancer therapy.
  • Ongoing radiation therapy.
  • Uncontrolled or active clinically relevant bacterial, fungal, or specific viral infection requiring systemic therapy.
  • Symptomatic spinal cord compression.
  • Evidence of active malignancy (other than study-specific malignancies) requiring systemic therapy within the next 2 years.
  • History or current evidence of retinal vein occlusion (RVO) or current risk factors for RVO.
  • Females who are pregnant or breastfeeding.
  • Actively receiving systemic treatment or direct medical intervention on another therapeutic clinical study.
  • Prior use of experimental agents that target the KRAS/BRAF/MEK/ERK pathway.

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