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临床试验/NCT05732831
NCT05732831
招募中
1 期

A Phase 1/2, Multi-Center, Open-Label Study to Evaluate the Safety, Tolerability, and Preliminary Anti-tumor Activity of TNG462 as a Single Agent and in Combination in Patients With MTAP-deleted Advanced or Metastatic Solid Tumors

Tango Therapeutics, Inc.53 个研究点 分布在 3 个国家目标入组 225 人2023年5月26日

概览

阶段
1 期
干预措施
TNG462
疾病 / 适应症
Locally Advanced Solid Tumor
发起方
Tango Therapeutics, Inc.
入组人数
225
试验地点
53
主要终点
Phase 1 Maximum Tolerated Dose
状态
招募中
最后更新
11天前

概览

简要总结

This is a first in human study in patients with advanced or metastatic solid tumors known to have an MTAP deletion. The first part of the study is an open-label, dose escalation and the second part is an open label dose expansion in specific MTAP-deleted tumor types. The study drug, TNG462, is a selective PRMT5 inhibitor administered orally. The study is planned to treat up to 225 participants.

详细描述

This is a Phase 1/2 multi-center, open label study in solid tumor patients who have a confirmed homozygous MTAP deletion in their tumor. The Phase 1 portion is a dose escalation study of oral TNG462 administered as a single agent and in combination with pembrolizumab in patients with confirmed MTAP-deleted solid tumors. In Phase 2, 6 expansion arms defined by confirmed MTAP-deleted tumor types will enroll in parallel at the RP2D(s) of TNG462 and in combination. In both parts of the study participants who tolerate the drug may continue treatment until disease progression.

注册库
clinicaltrials.gov
开始日期
2023年5月26日
结束日期
2026年9月1日
最后更新
11天前
研究类型
Interventional
研究设计
Sequential
性别
All

研究者

责任方
Sponsor

入排标准

入选标准

  • Age: ≥18 years-of-age at the time of signature of the main study ICF
  • Performance status: ECOG Performance Score of 0 to 1
  • Confirmed histologic or cytologic diagnosis of a locally advanced, metastatic, and/or unresectable solid tumor
  • Prior standard therapy, as available
  • Documented bi-allelic (homozygous) deletion of MTAP in a tumor detected by next- generation sequencing or absence of MTAP protein in a tumor detected by IHC.
  • Adequate organ function/reserve per local labs
  • Adequate liver function per local labs
  • Adequate renal function per local labs
  • Negative serum pregnancy test result at screening
  • Written informed consent must be obtained according to local guidelines

排除标准

  • Known allergies, hypersensitivity, or intolerance to TNG462, or its excipients or to pembrolizumab in the combination treatment arms
  • Uncontrolled intercurrent illness that will limit compliance with the study requirements
  • Active infection requiring systemic therapy
  • Currently participating in or has planned participation in a study of another investigational agent or device
  • Impairment of GI function or disease that may significantly alter the absorption of oral TNG462
  • Active prior or concurrent malignancy.
  • Central nervous system metastases associated with progressive neurological symptoms
  • Current active liver disease from any cause
  • Known to be HIV positive, unless all of the following criteria are met:
  • CD4+ count ≥300/μL

研究组 & 干预措施

Dose Expansion in Pancreatic Ductal Adenocarcinoma

Participants with MTAP-deleted pancreatic ductal adenocarcinoma will receive TNG462 at the identified RP2D(s)

干预措施: TNG462

Dose Expansion in Sarcoma

Participants with MTAP-deleted sarcoma (soft tissue or bone) will receive TNG462 at the identified RP2D(s)

干预措施: TNG462

Dose Expansion in Solid Tumors

Participants with other MTAP-deleted solid tumors will receive TNG462 at the identified RP2D(s)

干预措施: TNG462

Dose Expansion in NSCLC in Combination with Pembrolizumab

Participants NSCLC (squamous and non squamous) MTAP-deleted solid tumors will receive TNG462 at the identified RP2D(s)

干预措施: TNG462

Dose Expansion in NSCLC in Combination with Pembrolizumab

Participants NSCLC (squamous and non squamous) MTAP-deleted solid tumors will receive TNG462 at the identified RP2D(s)

干预措施: Pembrolizumab

Dose Expansion in Mesothelioma

Participants with MTAP-deleted mesothelioma will receive TNG462 at the identified RP2D(s)

干预措施: TNG462

Dose Escalation

Participants with MTAP-deleted solid tumors (excluding primary CNS) will receive escalating doses of TNG462 single agent and in combination with pembrolizumab to estimate the MTD

干预措施: TNG462

Dose Escalation

Participants with MTAP-deleted solid tumors (excluding primary CNS) will receive escalating doses of TNG462 single agent and in combination with pembrolizumab to estimate the MTD

干预措施: Pembrolizumab

Dose Expansion in NSCLC

Participants with MTAP-deleted NSCLC (squamous and non squamous) will receive TNG462 at the identified RP2D(s)

干预措施: TNG462

结局指标

主要结局

Phase 1 Maximum Tolerated Dose

时间窗: 28 days and 21 days

To determine the maximum tolerated dose (MTD) of TNG462 when administered as a single agent and in combination with pembrolizumab

Phase 1 Dosing Schedule

时间窗: 28 days

To determine the dosing schedule of TNG462

Phase 2 Anti-neoplastic Activity

时间窗: 16 weeks and 18 weeks

To assess anti-neoplastic activity of TNG462 administered single agent and in combination with pembrolizumab in patients with MTAP-deleted advanced solid tumors by RECIST v1.1, iRECIST or mRECIST v1.1

次要结局

  • Phase 1 Anti-neoplastic Activity(16 weeks)
  • Phase 1 and 2 Adverse Event Profile(28 days and 21 days)
  • Phase 1 and 2 Volume of Distribution(16 days)
  • Phase 1 and 2 Concentration versus Time Curve(16 days)
  • Phase 1 and 2 Time to Achieve Maximal Plasma Concentration(16 days)
  • Phase 1 and 2 Maximum Observed Plasma Concentration(16 days)
  • Phase 1 and 2 Terminal Elimination Half-life(16 days)
  • Phase 1 and 2 SDMA Levels(28 days)
  • Phase 1 and 2 Total Plasma Clearance(16 days)

研究点 (53)

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