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Clinical Trials/NCT05354843
NCT05354843
Recruiting
Phase 1

A Phase I, Open-Label, Multi-Center Dose Finding Study to Investigate the Safety, Pharmacokinetics, and Preliminary Efficacy of SHP2 Inhibitor ET0038 Monotherapy in Patients With Advanced Solid Tumors

Etern BioPharma (Shanghai) Co., Ltd2 sites in 1 country37 target enrollmentOctober 27, 2021
InterventionsET0038
DrugsET0038

Overview

Phase
Phase 1
Intervention
ET0038
Conditions
Advanced Solid Tumor
Sponsor
Etern BioPharma (Shanghai) Co., Ltd
Enrollment
37
Locations
2
Primary Endpoint
RP2D of Phase 2 Dose of ET0038
Status
Recruiting
Last Updated
4 years ago

Overview

Brief Summary

This is a Phase I, open-label, multi-center, dose-finding study to assess the safety, pharmacokinetics, and preliminary efficacy of ET0038 in patients with advanced solid tumors. It is anticipated that approximately 37 subjects will be enrolled in the dose-escalation phase of the study. ET0038 will be administered orally once daily (QD) in 21-day treatment cycles.

Detailed Description

This is an open-label, multicenter, Phase 1 study of oral ET0038 monotherapy in participants with advanced solid tumors. The study will include 2 components: 1) a Dose-Escalation Component for participants with advanced solid tumors and 2) a Dose-Expansion Component for participants with advanced solid tumors harboring certain specific mutations/rearrangements that result in hyperactivation of the RAS-MAPK pathway. Participants will be treated until disease progression per RECIST v1.1, unacceptable toxicity, or other criteria for withdrawal are met, whichever occurs first.

Registry
clinicaltrials.gov
Start Date
October 27, 2021
End Date
October 1, 2025
Last Updated
4 years ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Provision of signed and dated, written informed consent prior to any study specific procedures, sampling and analyses.
  • Aged at least 18 years at the time of ICF signature.
  • Histological or cytological confirmation of a solid tumor and have progressed despite standard therapy(ies), or are intolerant to standard therapy (ies), or have a tumor for which no standard therapy(ies) exists. Locally recurrent disease must not be amenable to surgical resection or radiotherapy with curative intent (patients who are considered suitable for surgical or ablative techniques following down-staging with study treatment are not eligible).
  • Estimated life expectancy of minimum of 12 weeks.
  • Patient with solid tumors must have at least 1 lesion, not previously irradiated, that can be accurately measured at pre-dose as ≥ 10 mm in the longest diameter (except lymph nodes which must have short axis ≥ 15 mm) with Computerised Tomography (CT) or magnetic resonance imaging (MRI) and which is suitable for accurate repeated measurements.
  • Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1 at ICF signature.
  • Males and Females of child-bearing potential must agree to use effective contraception from the time ICF signature until 12 weeks after the last dose. Females of childbearing potential include those who are premenopausal and those who are 2 years postmenopausal. Pregnancy tests for female of child-bearing potential must have a negative serum pregnancy test at Screening.

Exclusion Criteria

  • Central nervous system metastatic disease, leptomeningeal disease, or metastatic cord compression.
  • As judged by the investigator, any evidence of significant ophthalmological abnormalities including but not limited to history or current evidence of retinal vein occlusion (RVO) or current risk factors for RVO, retinal macular degeneration, uncontrolled glaucoma, cataract or marked decrease in visual acuity, symptomatic severe dry eye, conjunctivitis, or corneal ulcer.
  • Prior bone marrow or organ transplantation
  • Prior treatment with ET0038 or a SHP2 inhibitor.
  • Prior therapy with any investigational drugs or systemic anticancer treatment within 28 days (or a period of 5 'half-lives' of this investigational drugs or systemic anticancer treatment, whichever is the most appropriate and as judged by the investigator) at the time of ICF signature.
  • Radiotherapy with a wide field of radiation within 28 days, or radiotherapy with a limited field of radiation for palliation within 14 days at the time of ICF signature, or planning radical radiation therapy while participating in the study.
  • Prior major surgery (excluding placement of vascular access) within 28 days at the time of ICF signature, or planning for major surgery while participating in the study.
  • With the exception of alopecia, any unresolved toxicities from prior therapy greater than Common Terminology Criteria for Adverse Events (CTCAE5.0) Grade 1 at the time of ICF signature.
  • Any uncontrolled active infection requiring parenteral administration of antibiotics, antivirals, or antifungals at the time of ICF signature and/or within one week of Cycle 1 Day 1 (C1D1).
  • Patient with a history of active pulmonary tuberculosis infection within 1 year prior to screening (as judged by investigator, active pulmonary tuberculosis infection more than 1 year and no evidence of active pulmonary tuberculosis at present will be considering eligible)

Arms & Interventions

Dose Escalation and Dose Expansion

ET0038 will be administered orally once daily in 21 days treatment cycles.

Intervention: ET0038

Outcomes

Primary Outcomes

RP2D of Phase 2 Dose of ET0038

Time Frame: Approximately 2 years

Find RP2D

MTD of ET0038

Time Frame: Approximately 2 years

Fin MTD

Number of participants with adverse events (AEs)

Time Frame: Approximately 2 years

All patients participating in this study will be assessed for incidence and severity of adverse events (AEs) and serious AEs, including changes in laboratory values, vital signs, electrocardiograms, cardiac imaging and ophthalmological assessments

Secondary Outcomes

  • Disease Control Rate(Approximately 2 years)
  • Area under the curve(Approximately 2 years)
  • Cmax(Approximately 2 years)
  • Tmax(Approximately 2 years)
  • T1/2(Approximately 2 years)
  • Objective response rate(Approximately 2 years)
  • Duration of response(Approximately 2 years)
  • overall survival(Approximately 2 years)
  • progression-free survival(Approximately 2 years)

Study Sites (2)

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