Sym004 Versus Futuximab or Modotuximab in Patients With mCRC

Metastatic Colorectal Cancer Clinical Trial

Official title:

A Ph2, Randomized, Open-Label, Multicenter, Three-Arm Trial of Sym004 Versus Each of Its Component Futuximab and Modotuximab, in Patients With Chemotherapy-Refractory Metastatic Colorectal Carcinoma and Acquired Resistance to Anti-EGFR mAb

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03549338
• Other study ID #: Sym004-13
• Secondary ID: 2018-000618-39
• Status: Terminated
• Phase: Phase 2
• Start date: November 29, 2018
• Est. completion date: March 9, 2019

Study information

• Verified date: September 2020
• Source: Symphogen A/S
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a Phase 2, randomized, open-label, 3-arm trial in the ratio of 1:1:1 to either Sym004 (Arm A) versus each of its component monoclonal antibodies (mAbs), futuximab (Arm B) or modotuximab (Arm C), in genomically-selected patients with chemotherapy-refractory metastatic colorectal carcinoma (mCRC) and acquired resistance to anti-epidermal growth factor receptor (anti-EGFR) mAb therapy. The study is designed to evaluate the relative antitumor activity of each agent as assessed by imaging studies performed after 8 weeks of treatment.

Description:

Following consent and prior to randomization, genomic analysis will be conducted on blood samples obtained from each potential patient. Triple-negative (TN) results as defined in trial eligibility criteria will be required for initial eligibility. Patients with TNmCRC will continue in the screening process. Once deemed fully eligible, patients will be randomized to Arm A, Arm B, or Arm C.

Dosing cycles of 28 days will continue until documented disease progression (PD) or another criterion for discontinuation is met. Antitumor activity will be assessed at the end of every 2 cycles (every 8 weeks [Q8W]). At the End of Cycle 2 (EOC2) tumor assessment:

• Patients assigned to Arm A (Sym004) with a documented objective response (OR) or stable disease (SD) will continue to receive Sym004; patients at the EOC2 with documented PD will be discontinued from study

• Patients assigned to Arm B (futuximab) or Arm C (modotuximab) with a documented OR or SD will be crossed-over to receive Sym004; patients with documented PD at the EOC2 (or prior to the EOC2) will be offered the opportunity to crossover to receive Sym004 or will be discontinued from study

To be considered evaluable for antitumor activity assessment, patients must have completed 2 cycles of dosing inclusive of EOC2 disease imaging studies and must have received any amount of their assigned investigational medicinal product (IMP) during that period, or have PD documented by imaging studies prior to the EOC2. Non-evaluable patients and patients discontinuing from study prior to the EOC2 for reasons other than documented PD will not be replaced.

Note: In December 2018, the decision was made to terminate the trial and enrollment was prematurely discontinued. The primary, secondary, and exploratory objectives are no longer applicable. Only clinical safety-related evaluations will be conducted.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 2
• Est. completion date: March 9, 2019
• Est. primary completion date: March 1, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Male or female patients, = 18 years of age at the time of obtaining informed consent.

• Histologically- or cytologically-confirmed mCRC.

• Microsatellite instability-high (MSI-H) / mismatch repair-deficient (dMMR) tumors must have received prior therapy with pembrolizumab, nivolumab, or other programmed cell death protein-1 (PD-1)/programmed death-ligand 1 (PD-L1) pathway blocker, and must have progressed on that therapy.

• Meeting the protocol definition of TNmCRC assessed in the screening blood test.

• mCRC currently not amenable to surgical intervention due to either medical contraindications or non-resectability of the tumor.

• Measurable disease according to RECIST v1.1, and willingness to undergo a total of 2 biopsies of a primary or metastatic tumor site(s) considered safely accessible for biopsy.

• Must have received at least 2 prior regimens of standard chemotherapy for mCRC and must have been refractory to or failed (includes intolerance to) those regimens. Prior standard chemotherapy may not have included TAS-102 or regorafenib, but must have included agents as specified in the protocol.

• "Acquired" resistance to commercially available anti-EGFR mAbs approved for the treatment of mCRC must have:

1. Received treatment with an anti-EGFR for =16 weeks

2. Progressive disease (PD) documented by imaging or clinical findings less than or equal to 6 calendar months after cessation of previous anti-EGFR mAb treatment

3. No more than 6 calendar months from last dose of previous anti-EGFR mAb treatment to date of consent for this trial (regardless of the line of therapy in which it was used)

• Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1

• Not of childbearing potential or who agree to use a highly effective method of contraception during the study beginning within 2 weeks prior to the first dose and continuing until 3 months after the last dose of study drug.

Exclusion Criteria:

• Women who are pregnant or lactating or intending to become pregnant before, during, or within 3 months after the last dose of study drug.

• Prior history of specific mutations (specified in the protocol) in the tumor at the time of any previous assessment.

• Known, untreated central nervous system (CNS) or leptomeningeal metastases, or spinal cord compression; patients with any of these not controlled by prior surgery or radiotherapy, or patients with symptoms suggesting CNS involvement for which treatment is required

• An active second malignancy or history of another malignancy within the last 5 years, with exceptions.

• Active thrombosis, or a history of deep vein thrombosis (DVT) or pulmonary embolism (PE) within 4 weeks prior to first administration of study drug unless adequately treated and considered by the Investigator to be stable.

• Active uncontrolled bleeding or a known bleeding diathesis

• Known clinically significant cardiovascular disease or condition.

• Non-healing wounds on any part of the body.

• Significant gastrointestinal abnormality.

• Skin rash > Grade 1 from prior anti-EGFR therapy at the time of randomization.

• Unresolved > Grade 1 toxicity associated with any prior antineoplastic therapy

Drugs and Other Treatments Exclusion Criteria:

• Prior treatment with TAS-102 or regorafenib

• Any antineoplastic agent for the primary malignancy (standard or investigational) without delayed toxicity within 4 weeks prior to first administration of IMP and during study with exceptions

• Any other investigational treatments within 4 weeks prior to and during study; includes participation in any medical device or other therapeutic intervention clinical trials

• Radiotherapy as specified in the protocol

• Immunosuppressive or systemic hormonal therapy (> 10 mg daily prednisone equivalent) within 2 weeks prior to first administration of IMP and during study; allowed therapies are specified in the protocol.

Related Conditions & MeSH terms

• Carcinoma
• Colorectal Cancer Metastatic
• Colorectal Neoplasms
• Metastatic Colorectal Cancer

Intervention

Drug:
• Sym004
Sym004 is a 1:1 mixture of two recombinant mAbs (futuximab and modotuximab) which bind specifically to non-overlapping epitopes located in the extracellular domain (ECD) of the EGFR.
• Futuximab
Futuximab is one of two mAb components that constitute Sym004.
• Modotuximab
Modotuximab is one of two mAb components that constitute Sym004.

Locations

Country	Name	City	State
Germany	Uniklinik Dresden	Dresden
Germany	Universitaetsklinikum Essen	Essen
Germany	Asklepios Kliniken Altona	Hamburg
Germany	Universitätsmedizin Mannheim	Mannheim
Germany	Städtisches Klinikum München	München
Italy	ASST Grande Ospedale Metropolitano Niguarda	Milano
Italy	Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale"	Napoli
Italy	Università degli Studi della Campania "Luigi Vanvitelli"	Napoli
Spain	Hospital del Mar	Barcelona
Spain	Institut Català d'Oncologia	Barcelona
Spain	Vall d'Hebron Institut d'Oncologia (VHIO)	Barcelona
Spain	Hospital Universitario HM Sanchinarro	Madrid
Spain	Hospital Clínico de Valencia	Valencia
United States	Emory University Hospital	Atlanta	Georgia
United States	Massachusetts General Hospital	Boston	Massachusetts
United States	University of North Carolina - Lineberger Comprehensive Cancer Center	Chapel Hill	North Carolina
United States	City of Hope - Comprehensive Cancer Center	Duarte	California
United States	The University of Texas MD Anderson Cancer Center	Houston	Texas

Sponsors (1)

Lead Sponsor	Collaborator
Symphogen A/S

Countries where clinical trial is conducted

United States,  Germany,  Italy,  Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Participants With Adverse Events (AEs) by Nature, Severity, and Occurrence.	Measured From Baseline to End of Trial Participation, as Assessed by the Common Terminology Criteria for AEs (Version 5) (CTCAE v5). AEs will be coded according to the Medical Dictionary for Regulatory Activities (MedDRA) terminology and the severity of the toxicities will be graded according to the CTCAE v5, where applicable.	4 months