Comparing Efficacy and Safety of Cetuximab (CinnaGen) Versus Erbitux® (Merck) in Metastatic Colorectal Cancer

Metastatic Colorectal Cancer Clinical Trial

Official title:

A Phase III, Randomized, Two-armed, Parallel, Double-blind, Active-controlled, Equivalency Clinical Trial of Cetuximab (CinnaGen Co.) Efficacy and Safety Compared With Erbitux (Merck Co.) and FOLFIRI for RAS Wild-type mCRC

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03391934
• Other study ID #: CET.CIN.HR.96 (III)
• Status: Recruiting
• Phase: Phase 3
• Start date: January 20, 2018
• Est. completion date: February 1, 2026

Study information

• Verified date: April 2023
• Source: Cinnagen
• Contact: Somayeh Amini, Pharm D
• Phone: 00982143473000
• Email: amini.s[@]orchidpharmed.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The study is designed as phase III, randomized, two armed, parallel, double blind (patient and assessor blinded), active controlled, and equivalency clinical trial with primary endpoint of Progression-Free Survival of Cetuximab® (produced by CinnaGen) compared with Erbitux® (Cetuximab, the reference drug) in patients with RAS wild-type Metastatic Colorectal Cancer with the allocation ratio of 2:1.Patients who met the following criteria could be recruited to receive the mentioned intervention randomly. Inclusion criteria: Male or female older than 18 years old, histologically confirmed adenocarcinoma of the colon or rectum which is metastatic, having one or more bi-dimensionally measurable lesions as defined by RECIST criteria, tumor that could not be resected for curative purposes,ECOG performance status score of 2 or less,life expectancy of longer than 3 months (clinical assessment),evidence of tumor EGFR expression (expanded wild-type RAS),adequate organ and marrow function as defined:

ANC ≥ 1,500/mm3 Plt ≥ 100,000/mm3 Hb ≥ 9 g/dL (may have had blood transfusions) AST/ALT ≤ 2.5 IULN or ≤ 5 IULN with known liver metastases Total bilirubin ≤ 1.5 IULN Serum Creatinine ≤ 1.5 IULN INR ≤ 1.5 and PTT ≤ 1.5 IULN

Description:

The study is designed as phase III, randomized, two armed, parallel, double blind (patient and assessor blinded), active controlled, and equivalency clinical trial with primary endpoint of Progression-Free Survival of Cetuximab® (produced by CinnaGen) compared with Erbitux® (Cetuximab, the reference drug) in patients with RAS wild-type Metastatic Colorectal Cancer with the allocation ratio of 2:1.Patients who met the following criteria could be recruited to receive the mentioned intervention randomly. Inclusion criteria: Male or female older than 18 years old, histologically confirmed adenocarcinoma of the colon or rectum which is metastatic, having one or more bi-dimensionally measurable lesions as defined by RECIST criteria, tumor that could not be resected for curative purposes,ECOG performance status score of 2 or less,life expectancy of longer than 3 months (clinical assessment),evidence of tumor EGFR expression (expanded wild-type RAS),adequate organ and marrow function as defined:

ANC ≥ 1,500/mm3 Plt ≥ 100,000/mm3 Hb ≥ 9 g/dL (may have had blood transfusions) AST/ALT ≤ 2.5 IULN or ≤ 5 IULN with known liver metastases Total bilirubin ≤ 1.5 IULN Serum Creatinine ≤ 1.5 IULN INR ≤ 1.5 and PTT ≤ 1.5 IULN

Patients who have previous exposure to an anti-EGFR therapy or irinotecan-based chemotherapy, radiotherapy, surgery (excluding previous diagnostic biopsy), or any investigational drug in the 30-day period before the start of treatment in our trial will be excluded from the study. Also, female patients who are pregnant or lactating, and patients with any history of another primary malignancy in the past five years, with the exception of non-melanoma skin cancer, and carcinoma in situ of uterine cervix, and patients with inability to comply with the study and/or follow up procedures will be excluded.The primary endpoint of the study is Progression-Free Survival (PFS) defined as the time from randomization to disease progression or death from any cause. The secondary endpoints of the study are Overall Survival (OS) defined as the time from date of randomization to date of death due to any cause, Objective Response Rate (ORR) defined as the sum of partial and complete responses, according to RECIST criteria and Time to Treatment Failure (TTF) is defined as the time from the date of randomization to the date of each of the following:

The treatment modalities did not destroy or modify the cancer cells, The tumor either became larger (disease progression) or stayed the same size after treatment, Discontinuation of treatment, Death from any cause

Safety and Immunogenicity will also be assessed during the study.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 234
• Est. completion date: February 1, 2026
• Est. primary completion date: November 30, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Male or female older than 18 years old

• Histologically confirmed adenocarcinoma of the colon or rectum which is metastatic

• Having one or more bi-dimensionally measurable lesions as defined by RECIST criteria

• Tumor that could not be resected for curative purposes

• ECOG performance status score of 2 or less

• Life expectancy of longer than 3 months (clinical assessment)

• Evidence of tumor EGFR expression (expanded wild-type RAS)

• Adequate organ and marrow function as defined:

ANC = 1,500/mm3 Plt = 100,000/mm3 Hb = 9 g/dL (may have had blood transfusions) AST/ALT = 2.5 IULN or = 5 IULN with known liver metastases Total bilirubin = 1.5 IULN Serum Creatinine = 1.5 IULN INR = 1.5 and PTT = 1.5 IULN

Exclusion Criteria:

• Previous exposure to an anti-EGFR therapy or irinotecan-based chemotherapy

• Radiotherapy, surgery (excluding previous diagnostic biopsy), or any investigational drug in the 30-day period before the start of treatment in our trial

• Female patients who are pregnant or lactating

• Patients with any history of another primary malignancy in the past five years, with the exception of non-melanoma skin cancer, and carcinoma in situ of uterine cervix

• Patients with history of allergic reactions attributed to compounds of similar chemical or biologic drugs as cetuximab, irinotecan, fluorouracil or leucovorin

• Adjuvant treatment that was terminated 6 months or less before the start of treatment in our trial

• Inability to comply with study and/or follow-up procedures.

Related Conditions & MeSH terms

• Colorectal Neoplasms
• Metastatic Colorectal Cancer

Intervention

Drug:
• Cetuximab + FOLFIRI
Cetuximab 400 mg/m2 will be administered in the first dose and 250 mg/m2 will be administered in the next doses every week. Irinotecan will be administered 180 mg/m2 biweekly. Leucovorin will be administered 400 mg/m2 biweekly.Fluorouracil will be administered 400 mg/m2 push, and 2400 mg/m2 as 46-h infusion biweekly.

Locations

Country	Name	City	State
Iran, Islamic Republic of	Taleqani Hospital	Tehran

Sponsors (1)

Lead Sponsor	Collaborator
Cinnagen

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Progression Free Survival (PFS)	PFS is defined as the time from the date of randomization to the first date of documentation progression (per investigator assessment) or death as a result of any cause.	PFS was measured from the start of chemotherapy to the date of disease progression or to the date of death if no progression whichever came first, assessed up to 26 weeks
Secondary	Overall Survival (OS)	Overall survival OS is defines as the time from date of randomization to date of death due to any cause	26 weeks after study start
Secondary	Objective Response rate	Tumor response was defined as partial and complete responses, according to the RECIST criteria.	26 weeks after study start
Secondary	Time of treatment failures	Time of treatment failures define as the time from the date of randomization to the date of each of the following,; The treatment modalities did not destroy or modify the cancer cell.; The tumor either became larger (disease progression) or stayed the same size after treatment,; Death from any cause; Discontinuation of treatment	26 weeks after study start
Secondary	Adverse events	Safety wills assess on the basis of reports of adverse events, laboratory-test results, and vital sign measurements. Adverse events were categorized According to the Common Toxicity Criteria of the National Cancer Institute, version 4.0, in which a grade of 1 indicates mild adverse events, a grade of 2 moderate adverse events, a grade of 3 serious adverse events, and a grade of 4 life-threatening adverse events	26 weeks after study start
Secondary	immunogenicity	antidrug antibody [ADA] and neutralizing antibody [nAb] assessment	26 weeks after study start

External Links

•   This protocol is planned to be registered according to program in Iran Registry of Clinical Trial (IRCT).