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ACTIVE NOT RECRUITING
NCT06551064
PHASE1

Assessment of PK Similarity of FYB206 in Comparison With Keytruda in Resected Stage II or III Melanoma Patients

Sponsor: Formycon AG

View on ClinicalTrials.gov

Summary

Melanoma is a kind of skin cancer that starts in the melanocytes. Melanocytes are cells that make the pigment that gives skin its colour. 'Resected' means the melanoma has been completely removed with surgery. Pembrolizumab is an anti-cancer therapy that works with the immune system to fight cancer cells. Some cancer cells develop a way to hide from the body's immune system and, thus, allow the cancer cells to spread and grow. Pembrolizumab helps the immune system recognize and kill these cancer cells that want to hide. Pembrolizumab is a biologic drug (produced by living organisms) available in the market under the brand name Keytruda. Keytruda is approved globally for the treatment of a variety of cancers and as an addon or after therapy to primary cancer treatment like surgery. This helps prevent the cancer from returning, improving overall survival. FYB206 is a proposed biosimilar to Keytruda. A biosimilar is not identical but very similar to its original biologic. Biosimilars are expected to have a similar effect and safety to the original biologic. To learn what happens to a drug once it is in the body is called pharmacokinetics (PK). PK for biosimilar drugs is expected to remain similar to the original biologic. This study is to show that PK of FYB206 is similar to the reference product Keytruda for patients with completely resected Stage IIB/IIC or Stage III melanoma.

Official title: A Randomized, Double-Blind, Multicenter, Pharmacokinetic Equivalence Clinical Trial of Adjuvant FYB206 (Keytruda Biosimilar Candidate) in Comparison With Keytruda (Pembrolizumab) to Demonstrate Pharmacokinetic Similarity in Patients With Completely Resected Stage IIB/IIC or Stage III Melanoma

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

96

Start Date

2024-07-01

Completion Date

2026-06-30

Last Updated

2025-09-04

Healthy Volunteers

No

Interventions

BIOLOGICAL

FYB206

FYB206 (Keytruda biosimilar candidate - test product) 200 mg administered as an IV infusion over 30 minutes on Day 1 of each cycle

BIOLOGICAL

Keytruda

Keytruda (reference product) 200 mg administered as an IV infusion over 30 minutes on Day 1 of each cycle

Locations (17)

Formycon Investigative Site

Sarajevo, Bosnia and Herzegovina

Formycon Investigative Site

Sofia, Bulgaria

Formycon Investigative Site

Tartu, Estonia

Formycon Investigative Site

Batumi, Georgia

Formycon Investigative Site

Kutaisi, Georgia

Formycon Investigative Site

Tbilisi, Georgia

Formycon Investigative Site

Kaunas, Lithuania

Formycon Investigative Site

Chisinau, Moldova

Formycon Investigative Site

Skopje, North Macedonia

Formycon Investigative Site

Krakow, Poland

Formycon Investigative Site

Lodz, Poland

Formycon Investigative Site

Bucharest, Romania

Formycon Investigative Site

Cluj-Napoca, Romania

Formycon Investigative Site

Belgrade, Serbia

Formycon Investigative Site

Kragujevac, Serbia

Formycon Investigative Site

Niš, Serbia

Formycon Investigative Site

Kyiv, Ukraine