ADCX-020 for the Treatment of Patients With Locally Advanced or Metastatic Cancers

NCT ID: NCT07238075

Last Updated: 2025-11-20

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: PHASE1
• Total Enrollment: 290 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2026-02-14
• Study Completion Date: 2029-11-30

Brief Summary

The purpose of this first-in-human study is to explore the safety, pharmacokinetics and effects of the study drug ADCX-020 in patients with advanced and metastatic solid tumors. ADCX-020 is an investigational anticancer therapy called antibody drug conjugate.

This study is set up in multiple parts. In the first part of the study, participants receive increasing doses of ADCX-020. Then 2 or more doses will be assessed to identify the optimal dose. This optimal dose is subsequently evaluated for effect on different cancer types.

Detailed Description

This is a first-in-human (FIH) open-label, multicenter, dose escalation and multiple cohort expansion Phase 1a/b study to investigate safety, tolerability, PK, pharmacodynamics, and preliminary efficacy of ADCX-020 monotherapy in participants with relapsed or refractory solid tumors, or who are intolerant to standard of care.

During dose escalation, Phase 1a, participants will receive escalating doses of ADCX-020 to identify the MTD based on the observation of DLTs. Intermediate and higher dose levels as well as alternative dosing regimens may be investigated during this part of the study.

Dose expansion, Phase 1b, will be initiated with a dose optimization of ADCX-020 using two or more dose levels of ADCX-020 and/or evaluating a different dosing regimen. Expansion in multiple cohorts is planned for selected patient populations using the RP2D.

Phase 1a will be overseen by a Dose Escalation Committee (DEC) and Phase 1b will be overseen by a Safety Review Committee (SRC).

Conditions

Advanced Malignancy; Advanced Solid Cancers; Metastatic Solid Tumors

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Phase 1a ADCX-020

Dose escalation of ADCX-020, intravenous

Group Type: EXPERIMENTAL

ADCX-020

Intervention Type: DRUG

ADC

Phase 1b: ADCX-020

Dose optimization and expansion of ADCX-020, intravenous

Group Type: EXPERIMENTAL

ADCX-020

Intervention Type: DRUG

ADC

Interventions

ADCX-020

ADC

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Male and female participants ≥ 18 years of age
• Ph1a: Locally advanced or metastatic solid tumor relapsed or PD following local standard treatments, for which no standard treatment is available
• Ph1b: Eligible patients should have only received prior lines of systemic therapy according to SoC in the advanced/metastatic setting (not counting neoadjuvant/adjuvant treatment if completed >6 months prior to recurrence)
• Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1
• Radiologically measurable disease by RECIST v1.1
• Mandatory adequate tumor tissue sample available
• Must have recovered from all clinically relevant toxicities from previous cancer therapies (to at least Grade 1, except for alopecia)

Exclusion Criteria

• Known allergies/hypersensitivity/intolerance to or contraindication to exatecan, or any excipient
• Phase 1b: Prior antibody drug conjugate exposure with a topoisomerase 1 inhibitor payload
• Uncontrolled or significant cardiac disease including left ventricular ejection fraction (LVEF) <50%, myocardial infarction or uncontrolled/unstable angina
• Has clinically active central nervous system (CNS) metastases
• Has a history of lung fibrosis or non-infectious interstitial lung disease (ILD)/pneumonitis that required steroids, has current ILD/pneumonitis, or where suspected ILD/pneumonitis cannot be ruled out by imaging at screening
• Active corneal disease, or history of corneal disease within 12 months prior to enrollment
• Other unacceptable abnormalities, medications or procedures as defined by protocol

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Adcytherix SAS

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Adcytherix

Role: STUDY_DIRECTOR

Adcytherix SAS

Central Contacts

Adcytherix SAS

Role: CONTACT

clinicaltrials@adcytherix.com

+31 628839232

Other Identifiers

2025-523959-65-00

Identifier Type: CTIS

Identifier Source: secondary_id

ADCX-020-01

Identifier Type: -

Identifier Source: org_study_id