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Spots Global Cancer Trial Database for Evaluation of Safety and Efficacy of Sodium Thiosulfate (BYON5667) Eye Drops to Reduce Ocular Toxicity in Cancer Patients Treated With SYD985

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Trial Identification

Brief Title: Evaluation of Safety and Efficacy of Sodium Thiosulfate (BYON5667) Eye Drops to Reduce Ocular Toxicity in Cancer Patients Treated With SYD985

Official Title: A Multicenter, Randomized, Double-blind, Placebo-controlled Trial With a Single Arm run-in Period to Evaluate the Safety and Efficacy of Sodium Thiosulfate (BYON5667) Eye Drops to Reduce Ocular Toxicity in Cancer Patients Treated With SYD985

Study ID: NCT04983238

Study Description

Brief Summary: This multicenter, randomized, double-blind, placebo-controlled trial with a single arm run-in period is to evaluate the safety and efficacy of sodium thiosulfate (BYON5667) eye drops to reduce ocular toxicity in cancer patients treated with the antibody-drug conjugate (ADC) SYD985

Detailed Description: This multicenter trial has a single arm run-in period followed by a randomized, placebo-controlled, double-blind comparative part. In the single arm part of the trial, patients with HER2-expressing locally advanced or metastatic solid tumours will be enrolled and treated with the antibody-drug conjugate (ADC) SYD985 once every 3 weeks until disease progression or unacceptable toxicity. All patients will receive concomitant BYON5667 eye drops. When the primary safety and efficacy analysis of the BYON5667 eye drops at Day 63 is favorable, the trial may continue to the comparative part in which patients with locally advanced or metastatic HER2-positive breast cancer will be treated with SYD985. Patients will be randomly assigned (1:1) to receive BYON5667 or placebo eye drops.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

University Hospital Antwerp, Antwerp, , Belgium

UZ Leuven, Leuven, , Belgium

Institut Bergonié, Bordeaux, , France

Centre Oscar Lambret, Lille, , France

Hôpital Saint Louis, Paris, , France

Vall d' Hebron, Barcelona, , Spain

ICO I'Hospitalet - Hospital Duran i Reynals, L'Hospitalet De Llobregat, , Spain

Hospital Universitari Arnau de Vilanova, Lleida, , Spain

START Madrid HU Fundacion Jimenez Diaz, Madrid, , Spain

START Madrid HU HM Sanchinarro, Madrid, , Spain

Contact Details

Name: Ellen Mommers, PhD

Affiliation: Byondis B.V., The Netherlands

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

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