A First-in-human Dose-escalation and Expansion Study With the Antibody-drug Conjugate SYD1875

NCT ID: NCT04202705

Last Updated: 2023-01-30

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 31 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-02-28
• Study Completion Date: 2023-01-26

Brief Summary

This is the first-in-human study with SYD1875, an antibody-drug conjugate (ADC) comprising of a humanized IgG1 monoclonal antibody directed against the 5T4 oncofetal antigen covalently conjugated to a duocarmycin-based linker-drug. This study includes a dose-escalation part (Part 1) in which the maximum tolerated dose (MTD) and recommended dose for expansion (RDE) will be determined, and an expansion part (Part 2) to evaluate efficacy and safety in specific patient cohorts.

Detailed Description

Cancer cells can have different kinds of proteins on their cell surface; one of these is the oncofetal antigen 5T4. 5T4 plays an important role in the development of cancer. Currently no drugs are available that work via the 5T4 antigen.

The new cancer drug SYD1875 is being developed by Byondis B.V. SYD1875 is an antibody-drug conjugate and consists of two parts: an antibody and a linker-drug moiety containing a toxin. The antibody part binds to 5T4 on the surface of the cancer cell. When SYD1875 binds to this cancer cell, it will be internalized by the cell. After proteolytic cleavage of the linker, the toxin will be split off in the cell and the cancer cell will be killed. Thus, SYD1875 can be considered as a form of targeted chemotherapy.

This is the first study in which SYD1875 is administered to humans. The study consists of two parts:

Part 1 is the dose-escalation part in which a low dose of SYD1875 is given to cancer patients. If it is well tolerated, a higher dose of SYD1875 will be given to other cancer patients until the maximum tolerated dose is reached.

In Part 2 of the study, groups of patients with a specific type of cancer will receive the SYD1875 dose which has been selected for further evaluation.

All patients from both parts of the study will receive SYD1875 infusions every three weeks until progression of the cancer or unacceptable toxicity develops.

Conditions

Solid Tumor

Study Design

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

Study Groups

SYD1875

5T4-targeting Antibody-Drug Conjugate

Group Type: EXPERIMENTAL

SYD1875

Intervention Type: DRUG

SYD1875 IV (in the vein) infusion every three weeks. Number of cycles: until cancer progression or unacceptable toxicity develops. Different doses.

Interventions

SYD1875

SYD1875 IV (in the vein) infusion every three weeks. Number of cycles: until cancer progression or unacceptable toxicity develops. Different doses.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Patient with histologically-confirmed, locally advanced or metastatic cancer who has progressed on standard therapy or for whom no standard therapy exists, with the following restriction:
• Part 1: solid tumours of any origin
• Part 2: three patient cohorts
• Tumour 5T4 membrane staining according protocol
• Eastern Cooperative Oncology Group (ECOG) performance status ≤ 1;
• Adequate organ function
• For Part 2: measurable disease

Exclusion Criteria

• Having been treated with:

1. 5T4-targeting therapy at any time

2. Trastuzumab duocarmazine (SYD985) at any time

3. Other anticancer therapy within 4 weeks or as defined in the protocol

4. Hormone therapy within 1 week

• History or presence of keratitis, clinically significant renal disease, lung disease, or cardiovascular disease as specified in the protocol
• Symptomatic brain metastases, brain metastases requiring steroids or treatment for brain metastases within 8 weeks

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

Sponsors

Byondis B.V.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Ellen Mommers, PhD

Role: STUDY_DIRECTOR

Byondis B.V., The Netherlands

Locations

Institut Jules Bordet

Brussels, , Belgium

Institut Bergonié

Bordeaux, , France

Centre Oscar Lambret

Lille, , France

Countries

Belgium; France

Other Identifiers

SYD1875.001

Identifier Type: -

Identifier Source: org_study_id