Pembrolizumab (MK-3475) as Maintainance in Treated Patients With Unresectable Stage III NSCLC

NCT03379441 | Unknown Phase 2 FDA Drug

• 1 other identifier: 2016-001252-22
• Study Type: interventional
• Target: 126
• Locations: 1 country
• Sites: 14

Brief Summary

Maintainance therapy in patients with unresectable stage III, NSCLC Stage IIIA-B, unresectable, NSCLC, treated with definitive Chemo-Radiotherapy

Conditions

Non Small Cell Lung Cancer Patients

Outcome Measures

Primary Outcomes (1)

• OS

  The primary objective is to evaluate if treatment with chemo-radiotherapy followed by Pembrolizumab (MK-3475) maintenance (up to 24 months) results in superior Overall Survival (OS) in stage IIIA-B, unresectable, NSCLC compared to chemo-radiotherapy (CT-RT) followed by observation

  up to 24 months per patient

Secondary Outcomes (1)

• PFS

  up to 24 months per patient

Study Arms (2)

Experimental

EXPERIMENTAL

Pembrolizumab 200 mg Q3W IV infusion Day 1 of each 3 week cycle until: * PD, * unacceptable toxicity, * investigator choice, * patients IC withdrawal, * up to a maximum of 24 months (35 administrations) Experimental

Drug: Pembrolizumab Injectable Product

Observation

NO INTERVENTION

Interventions

Pembrolizumab Injectable Product DRUG

Pembrolizumab Injectable Product 200 mg Q3W Intravenous

Experimental

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Be willing and able to provide written informed consent/assent for the trial.
• Be \> 18 years of age on day of signing informed consent.
• Have measurable disease based on RECIST 1.1.
• Be willing to provide tissue from a newly obtained core, trucut biopsy or excisional biopsy of a tumor lesion. Newly-obtained is defined as a specimen obtained up to 6 weeks (42 days) prior to initiation of treatment on Day 1. Subjects for whom newly-obtained samples cannot be provided (e.g. inaccessible or subject safety concern) may submit an archived specimen only upon agreement from the PI.
• Have a performance status of 0 or 1 on the ECOG Performance Scale.
• Demonstrate adequate organ function , all screening labs should be performed within 10 days of treatment initiation.
• Female subject of childbearing potential should have a negative urine or serum pregnancy within 72 hours prior to receiving the first dose of study medication. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required.
• Female subjects of childbearing potential should be willing to use 2 methods of birth control or be surgically sterile, or abstain from heterosexual activity for the course of the study through 120 days after the last dose of study medication (Section 8.14.2). Subjects of childbearing potential are those who have not been surgically sterilized or have not been free from menses for \> 1 year.
• Male subjects should agree to use an adequate method of contraception starting with the first dose of study therapy through 120 days after the last dose of study therapy

You may not qualify if:

• Is currently participating and receiving study therapy or has participated in a study of an investigational agent and received study therapy or used an investigational device within 4 weeks of the first dose of treatment.
• Has a diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior to the first dose of trial treatment.
• Has a known history of active Bacillus Tuberculosis (TB)
• Hypersensitivity to pembrolizumab or any of its excipients.
• Has had a prior anti-cancer monoclonal antibody (mAb) within 4 weeks prior to study Day 1 or who has not recovered (i.e., ≤ Grade 1 or at baseline) from adverse events due to agents administered more than 4 weeks earlier.
• Has a known additional malignancy that is progressing or requires active treatment. Exceptions include basal cell carcinoma of the skin or squamous cell carcinoma of the skin that has undergone potentially curative therapy or in situ cervical cancer.
• Has active autoimmune disease that has required systemic treatment in the past 2 years (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive drugs). Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment.
• Has a history of (non-infectious) pneumonitis that required steroids or current pneumonitis, or has evidence of interstitial lung disease.
• Has an active infection requiring systemic therapy.
• Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the subject's participation for the full duration of the trial, or is not in the best interest of the subject to participate, in the opinion of the treating investigator.
• Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.
• Is pregnant or breastfeeding, or expecting to conceive or father children within the projected duration of the trial, starting with the pre-screening or screening visit through 120 days after the last dose of trial treatment.
• Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent.
• Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies).
• Has known active Hepatitis B (e.g., hepatitis B virus surface antigen \[HBsAg\] reactive) or Hepatitis C (e.g., HCV ribonucleic acid \[RNA\] qualitative is detected).

Sponsors & Collaborators

• University of Turin, Italy: lead

Study Sites (14)

CRO Aviano

Aviano, Pordenone, 33081, Italy

Location

AOU San Luigi- Department of Oncology

Orbassano, Turin, 10043, Italy

Location

Istituto Tumori Giovanni Paolo II

Bari, 70124, Italy

Location

Chieti Università degli Studi "G. D'Annunzio"

Chieti, 66100, Italy

Location

AOU Careggi

Florence, 50134, Italy

Location

IRCCS AO San Martino

Genova, 16132, Italy

Location

Azienda Ospedaliera Papardo

Messina, 98158, Italy

Location

Istituto Clinico Humanitas

Milan, 20089, Italy

Location

Ospedale San Raffaele

Milan, 20132, Italy

Location

Policlinico Modena

Modena, Italy

Location

Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale"

Napoli, 80131, Italy

Location

Policlinico Universitario Campus Biomedico

Roma, 00128, Italy

Location

PO Centrale

Taranto, 74100, Italy

Location

Policlinico Verona Borgo Roma

Verona, 37134, Italy

Location

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Who Masked: PARTICIPANT, INVESTIGATOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Principal Investigator

Study Record Dates

• First Submitted: November 23, 2017
• First Posted: December 20, 2017
• Study Start: January 1, 2018
• Primary Completion: January 1, 2023
• Study Completion: January 1, 2023
• Last Updated: December 22, 2017

Record last verified: 2017-12

Locations

IT (14)