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Spots Global Cancer Trial Database for Safety, Immunogenicity and Preliminary Clinical Activity Study of PDC*lung01 Cancer Vaccine in NSCLC

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Trial Identification

Brief Title: Safety, Immunogenicity and Preliminary Clinical Activity Study of PDC*lung01 Cancer Vaccine in NSCLC

Official Title: An Open-label, Dose-escalation, Phase I/II Study to Assess the Safety, the Tolerability, the Immunogenicity and the Preliminary Clinical Activity of the Therapeutic Cancer Vaccine, PDC*lung01, Associated or Not With Anti-PD-1 Treatment in Patients With Non-small-cell Lung Cancer (NSCLC)

Study ID: NCT03970746

Study Description

Brief Summary: PDC-LUNG-101 trial is an open-label, dose-escalation, phase I/II study to assess the safety, the tolerability, the immunogenicity and the preliminary clinical activity of the therapeutic cancer vaccine, PDC\*lung01, associated or not with anti-PD-1 treatment in patients with non-small-cell lung cancer.

Detailed Description: The therapeutic cancer vaccine, PDC\*lung01 will be administered at two dose levels (low dose (LD) and high dose (HD)), as single agent or during maintenance treatment by pemetrexed (for adenocarcinomas in Cohorts A1 and A2) or added to the SoC (cohorts B1 and B2) i.e. anti-PD-1. In cohorts A1 (low dose cohort) and A2 (high dose cohort), NSCLC patients will be treated at each of the six PDC\*lung01 treatment visits with low dose/high dose administered successively by subcutaneous and then by intravenous route. In cohort B1 and B2, the first PDC\*lung01 injection will start within 48 hours after the first infusion of anti-PD-1. The fourth PDC\*lung01 injection will occur within 48 hours after the infusion of the second cycle of anti-PD-1. For each patient, the study will be divided into three consecutive parts: * Pre-screening (for HLA-A\*02:01 positivity), only patients with positive HLA-A\*02:01 status will be proposed to be screened. * Active period comprising a screening period, a treatment period (visits V1 to V6, during which the patient receives PDC\*lung01 vaccine, at each visit), a V7 one week after the last injection and an end-of-treatment (EoT) visit (V8, 4 weeks after the last injection), * Follow-up period which starts after the EoT visit and lasts up to two years after the first IMP administration.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Grand Hôpital de Charleroi, Charleroi, , Belgium

Jessa Ziekenhuis, Hasselt, , Belgium

AZ Groeninge, Kortrijk, , Belgium

University Hospitals KU Leuven, Leuven, , Belgium

CHU Liège- Sart Tilman, Liège, , Belgium

AZ Delta vzw, Roeselare, , Belgium

AZ Sint-Nikolaas, Sint-Niklaas, , Belgium

CHU Grenoble, Grenoble, , France

Centre Léon Bérard, Centre de lutte contre le cancer, Lyon, , France

CHU Nantes, Nantes, , France

Universitätsklinikum Franlkfurt, Frankfurt am main, , Germany

Kliniken der Stadt Köln GmbH, Köln, , Germany

Jeroen Bosch Ziekenhuis - 's hertogenbosch, 's Hertogenbosch, , Netherlands

Antoni Van Leeuwenhoek (Nederlands Kanker Instituut), Amsterdam, , Netherlands

Leiden University Medical Center (LUMC), Leiden, , Netherlands

University Clinical Centre, Gdańsk, , Poland

Contact Details

Name: Johan Vansteenkiste, Prof

Affiliation: KU Leuven

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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