A Phase 1a/b Study of ADRX-0706 in Subjects With Select Advanced Solid Tumors

INTRODUCTION

  • Org Study ID: ADRX-0706-001
  • Secondary ID: N/A
  • NCT ID: NCT06036121
  • Sponsor: Adcentrx Therapeutics

BRIEF SUMMARY

The primary purpose of this study is to assess the safety, tolerability, and pharmacokinetics, and to identify the optimal dose of ADRX-0706 in patients with select advanced solid tumors.

DETAILED DESCRIPTION

This is a 2 part study. The Phase 1a will consist of a dose escalation of ADRX-0706 to evaluate initial safety and tolerability in patients with select advanced solid tumors, and to identify the recommended dose to be used in the Phase 1b. The Phase 1b will further evaluate the safety and tolerability, as well as preliminary efficacy, and identify the optimal dose of ADRX-0706 in patients with urothelial cancer, triple negative breast cancer, and cervical cancer.

  • Overall Status
    Active, not recruiting
  • Start Date
    September 26, 2023
  • Phase
    Phase 1
  • Study Type
    Interventional

PRIMARY OUTCOMES

Primary Outcome 1 - Measure: Incidence of adverse events

Primary Outcome 1 - Timeframe: Until study completion (estimated 3 years)

CONDITION

  • Solid Tumors
  • Triple Negative Breast Cancer (TNBC)
  • Urothelial Cancer
  • Cervical Cancer

ELIGIBILITY

Inclusion Criteria:
* Phase 1a Dose Escalation: Subjects with histologically confirmed select advanced solid tumors, including urothelial carcinoma (UC), head and neck squamous cell carcinoma (HNSCC), breast cancer, cervical cancer, ovarian cancer, non-small cell lung cancer (NSCLC), and pancreatic cancer. Subjects must have received at least one prior systemic regimen and have no other therapy available known to provide meaningful clinical benefit in the opinion of the investigator.

- * Phase 1b Dose Expansion: Subjects with urothelial cancer, triple negative breast cancer or cervical cancer with disease progression after at least one prior systemic regimen and no standard treatment options available and considered appropriate in the opinion of the investigator, unless subject refuses standard therapy.

- * Measurable disease according to RECIST version 1.1

- * Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1

- * Adequate hematologic, liver, and renal function
Exclusion Criteria:
* Active and uncontrolled central nervous system metastases

- * Significant cardiovascular disease

- * History of another malignancy other than the one for which the subject is being treated on this study within 3 years

- * Receipt of any anticancer or investigational therapy within 5 elimination half-lives or 14 days (whichever is less)

- * Any P-gp inducers/inhibitors or strong CYP3A inhibitors received within 14 days prior to the first dose of study drug

- * Receiving systemic antimicrobial treatment for active infection; routine antimicrobial prophylaxis is permitted

Gender: All

Minimum Age: 18 Years

Maximum Age: N/A

Healthy Volunteers: No

OFFICIAL INFORMATION

Name: N/A

Role: N/A

Affiliation: N/A

Overall Contact

Name: N/A

Phone: N/A

Email: N/A

LOCATION

Facility Status Contact