- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04069936
Marrow Infiltrating Lymphocytes - Non-Small Cell Lung Cancer (MILs™ - NSCLC) Alone or in Combination With Nivolumab With or Without Tadalafil in Locally Advanced and Unresectable or Metastatic NSCLC
July 28, 2022 updated by: WindMIL Therapeutics
A Phase 2a, Open-Label, Multi-Center Study to Assess the Efficacy and Safety of Marrow Infiltrating Lymphocytes - Non-Small Cell Lung Cancer (MILs™ - NSCLC) Alone or in Combination With Nivolumab With or Without Tadalafil in Subjects With Locally Advanced and Unresectable or Metastatic NSCLC Previously Treated With Anti-PD-1
The purpose of this study is to determine the safety and efficacy of MILs™ - NSCLC alone and in combination with nivolumab with or without tadalafil in subjects with locally advanced and unresectable or metastatic NSCLC who are refractory or relapsing to a PD-1 containing regimen.
Study Overview
Status
Terminated
Conditions
Intervention / Treatment
Detailed Description
This study will examine the safety and efficacy of Marrow Infiltrating Lymphocytes-Non-Small Cell Lung Cancer (MILs™ - NSCLC) combined with nivolumab with or without tadalafil in subjects with locally advanced and unresectable and metastatic NSCLC who were refractory to, or have relapsed on, an anti-PD-1 containing regimen.
MILs™ - NSCLC are an adoptive cell therapy product derived via the activation and expansion of bone marrow T cells.
Subjects will have bone marrow harvested during the Screening Period which will be used to manufacture the MILs™ - NSCLC.
The MILs™ - NSCLC will then be administered on Day 0. Nivolumab will be administered on Day 1 and will continue every four weeks until treatment discontinuation.
Tadalafil will be administered on Day 1 and will continue daily until treatment discontinuation.
Study Type
Interventional
Enrollment (Actual)
19
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
California
-
Duarte, California, United States, 91010
- City of Hope
-
Los Angeles, California, United States, 90095
- University of California - Los Angeles
-
-
Florida
-
Tampa, Florida, United States, 33612
- Moffitt Cancer Center
-
-
Georgia
-
Atlanta, Georgia, United States, 30322
- Emory University
-
-
Michigan
-
Detroit, Michigan, United States, 48201
- Karmanos Cancer Center
-
-
Missouri
-
Saint Louis, Missouri, United States, 63110
- Washington University
-
-
Nebraska
-
Omaha, Nebraska, United States, 68198
- University of Nebraska Medical Center
-
-
Ohio
-
Cleveland, Ohio, United States, 44195
- Cleveland Clinic
-
-
Pennsylvania
-
Philadelphia, Pennsylvania, United States, 19111
- Fox Chase Cancer Center
-
-
Tennessee
-
Nashville, Tennessee, United States, 37203
- Sarah Cannon Research Institute
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Eastern Cooperative Oncology Group (ECOG) Performance Status 0 or 1.
- Locally advanced and unresectable, or metastatic NSCLC.
- Histologically or cytologically confirmed, either squamous or non-squamous NSCLC.
- Measurable disease as per RECIST 1.1
- Willingness to undergo bone marrow aspiration (BMA).
No more than one treatment regimen following an anti-PD-1 antibody containing treatment regimen prior to BMA collection.
a. Subjects may have BMA collected while on an anti-PD-1 antibody containing treatment regimen or while on a treatment regimen immediately following an anti-PD-1 antibody containing treatment regimen.
- BMA may be collected while on an anti-PD-1 antibody containing treatment regimen or while on a treatment regimen immediately following an anti-PD-1 antibody containing treatment regimen. However, the subjects must have radiographic evidence of disease progression prior to lymphodepletion.
- ≥ 21 days have lapsed since last cytotoxic chemotherapy treatment prior to collection of the BMA.
- Previous treatment with the appropriate targeted therapy if the subject has known EGFR/ALK/ROS1 rearrangements.
- Willingness to provide a fresh tumor biopsy during Screening Period or formalin-fixed, paraffin-embedded tissue collected at the time of most recent relapse. Note: Archival tissue regardless of biopsy date may be considered.
- Adequate renal, hepatic and bone marrow function defined as total bilirubin </= 1.5 x ULN (except for subjects with Gilbert's disease ≤ 3.0 x ULN with direct bilirubin </= 1.5 x ULN ). Aminotransferase (AST) / Alanine Aminotransferase (ALT) </= 3.0 X ULN (subjects with liver involvement will be allowed </= 5.0 X ULN). Serum creatinine </= 1.5 x ULN; if serum creatinine is 1.5 to 2.0 × ULN, then the creatinine clearance (calculated using the Cockcroft-Gault formula or measured) must be ≥ 40 mL/min. Lymphocyte >/= 0.7 x 10^9/L. ANC >/= 1.5 x 10^9/L. Platelets >/= 100 × 10^9/L. WBC >/= 2.0 ×10^9/L. Hemoglobin > 9.0 g/dL.
- Women of childbearing potential and male subjects (even if they are surgically sterilized or had a vasectomy) and their partners must agree to abstain or to use an effective form of birth control during the study for at least 6 months following administration of the last dose of lymphodepletion or for at least 5 months following the last dose of nivolumab for females and 7 months for males, whichever is longer. In addition, male subjects must not donate sperm during this period.
- Capable of giving and has provided a signed ICF, which includes compliance with the requirements and restrictions listed in the ICF and in this protocol.
Exclusion Criteria:
- Insufficient activation/expansion of T cells or other problems with the subject's MILs™ - NSCLC product which would prohibit administration.
- Major surgical procedure within 7 days of the first dose of lymphodepletion treatment.
- Prior malignancy active within the previous 3 years from date of BMA collection except for locally curable cancers that have been apparently cured, such as basal or squamous cell skin cancer, superficial bladder cancer, or carcinoma in situ of the prostate, cervix, or breast.
- Subjects with symptomatic uncontrolled brain metastases requiring treatment with steroids or anti-seizure medications within 28 days prior to the BMA are excluded. However, participants with brain metastases that have been previously treated and are stable on subsequent scan(s) are allowed and subjects with untreated possible brain metastases that are new at the time of screening and are < 1 cm and asymptomatic are allowed. Subjects with asymptomatic untreated CNS disease may undergo BMA prior to treatment of such disease.
- Infection requiring treatment with intravenous antibiotics, antifungal, or antiviral agents within 7 days prior to the BMA.
- Presence of an autoimmune disease requiring active systemic treatment.
- Clinically significant, uncontrolled cardiovascular disease, including congestive heart failure Grade III or IV according to the New York Heart Association classification, myocardial infarction or unstable angina within the previous 6 months prior to BMA collection.
- Known diagnosis of human immunodeficiency virus (HIV) or active viral hepatitis.
- Administration of neutrophil growth factor support within 14 days prior to the BMA.
- Use of systemic corticosteroids (glucocorticoids) for greater than one day within 28 days prior to the BMA.
- Planned use of systemic corticosteroids (glucocorticoids) for greater than one day within 28 days prior to MILs™ - NSCLC administration.
- Prior radiation to both sides of the pelvis. Prior radiation to one side of the pelvis is permitted as long as the other side of the pelvis.
- Subjects with history of life-threatening toxicity related to prior immune therapy except those that are unlikely to re-occur with standard countermeasures.
- Receipt of live attenuated vaccine within 30 days of planned Day 0.
- History of allergy or hypersensitivity to MILs™-NSCLC, cyclophosphamide, fludarabine, nivolumab, tadalafil or their components.
- Pregnant or lactating females.
- Prior or ongoing clinically significant illness, medical condition, surgical history, physical finding, or laboratory abnormality that, in the Investigator's opinion, could affect the safety of the subject or impair the assessment of study results.
- Unwilling or unable to comply with the protocol.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Sequential Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: MILs™ - NSCLC plus nivolumab with or without tadalafil
Locally advanced and unresectable and metastatic NSCLC subjects previously treated with anti-programmed cell death-1 (PD-1) will be treated with MILs™ - NSCLC plus nivolumab with or without tadalafil.
|
To evaluate the safety of MILs™ - NSCLC alone in subjects with locally advanced and unresectable or metastatic NSCLC
Other Names:
To evaluate the efficacy of MILs™ - NSCLC in combination with nivolumab in subjects with locally advanced and unresectable or metastatic NSCLC
To evaluate the efficacy of MILs™ - NSCLC in combination with nivolumab with or without tadalafil in subjects with locally advanced and unresectable or metastatic NSCLC
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Adverse Events per National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events version 5.0
Time Frame: From ICF through 100 days after the last dose of study treatment
|
Incidence, intensity, and type of AE
|
From ICF through 100 days after the last dose of study treatment
|
Serious Adverse Events per NCI-CTCAE version 5.0
Time Frame: From ICF through 100 days after the last dose of study treatment
|
Incidence, intensity, and type of SAE
|
From ICF through 100 days after the last dose of study treatment
|
Overall Response Rate (ORR) of MILs™ - NSCLC in combination with nivolumab with or without tadalafil
Time Frame: 24 months
|
Proportion of subjects with reduction in tumor burden of a predefined amount per RECIST 1.1
|
24 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Duration of response
Time Frame: up to 5 years after treatment discontinuation
|
Duration from first documented evidence of CR or PR until the first documented evidence of PD or death due to any cause, whichever occurs first
|
up to 5 years after treatment discontinuation
|
Disease control rate
Time Frame: up to 5 years after treatment discontinuation
|
Proportion of subjects in the efficacy population who achieve an Investigator-assessed confirmed CR, PR, or SD per RECIST 1.1
|
up to 5 years after treatment discontinuation
|
Progression-free survival
Time Frame: up to 5 years after treatment discontinuation
|
Date of first the administration of MILs™ - NSCLC until documented PD or death due to any cause, whichever occurs first
|
up to 5 years after treatment discontinuation
|
Overall survival
Time Frame: up to 5 years after treatment discontinuation
|
Duration from the date of administration of MILs™ - NSCLC until death due to any cause
|
up to 5 years after treatment discontinuation
|
Overall Response Rate (ORR) of MILs™ - NSCLC
Time Frame: 24 months
|
Proportion of subjects with reduction in tumor burden of a predefined amount per RECIST 1.1
|
24 months
|
Safety of MILs™ - NSCLC alone and in combination with nivolumab with or without tadalafil as assessed by vital signs (pulse rate)
Time Frame: From ICF through 100 days after the last dose of study treatment
|
Pulse rate in beats/minute
|
From ICF through 100 days after the last dose of study treatment
|
Safety of MILs™ - NSCLC alone and in combination with nivolumab with or without tadalafil as assessed by vital signs (weight)
Time Frame: From ICF through 100 days after the last dose of study treatment
|
Weight in pounds
|
From ICF through 100 days after the last dose of study treatment
|
Safety of MILs™ - NSCLC alone and in combination with nivolumab with or without tadalafil as assessed by vital signs (blood pressure)
Time Frame: From ICF through 100 days after the last dose of study treatment
|
Systolic and diastolic blood pressure in mmHg
|
From ICF through 100 days after the last dose of study treatment
|
Safety of MILs™ - NSCLC alone and in combination with nivolumab with or without tadalafil as assessed by vital signs (respiratory rate)
Time Frame: From ICF through 100 days after the last dose of study treatment
|
Respiratory rate in breaths/minute
|
From ICF through 100 days after the last dose of study treatment
|
Safety of MILs™ - NSCLC alone and in combination with nivolumab with or without tadalafil as assessed by vital signs (temperature)
Time Frame: From ICF through 100 days after the last dose of study treatment
|
Termperature in Fahrenheit
|
From ICF through 100 days after the last dose of study treatment
|
Safety of MILs™ - NSCLC alone and in combination with nivo. with or w/o tadalafil by liver function (ALT/AST (U/L), albumin (g/dL), tot. bilirubin (mg/dL)), kidney function (creatinine (mg/dL) and endocrine function (T3 free and T4 free (ng/dL))
Time Frame: From ICF through 100 days after the last dose of study treatment
|
Clinical chemistry results will be summarized and changes from baseline provided
|
From ICF through 100 days after the last dose of study treatment
|
Safety of MILs™ - NSCLC alone and in combination with nivolumab with or without tadalafil by cell count (e.g. RBC (10^6/uL), WBC (10^3/uL), absolute cell count (10^3/uL), Hct (%) and Hgb (g/dL)
Time Frame: From ICF through 100 days after the last dose of study treatment
|
Hematology results will be summarized and changes from baseline provided
|
From ICF through 100 days after the last dose of study treatment
|
Safety of MILs™ - NSCLC alone and in combination with nivolumab with or without tadalafil as assessed by APTT (seconds), fibrinogen (mg/dL), INR and protime (seconds)
Time Frame: From ICF through 100 days after the last dose of study treatment
|
Coagulation results will be summarized in data listings
|
From ICF through 100 days after the last dose of study treatment
|
Safety of MILs™ - NSCLC alone and in combination with nivolumab with or without tadalafil as assessed by urine appearance, color, pH, specific gravity and presence of blood, bilirubin, glucose, ketone, leukocyte esterase, nitrite, protein, urobilinogen
Time Frame: From ICF through 100 days after the last dose of study treatment
|
Urinalysis results will be summarized in data listings
|
From ICF through 100 days after the last dose of study treatment
|
Safety of MILs™ - NSCLC alone and in combination with nivolumab with or without tadalafil by electrocardiograms (ECGs) assessed by Investigators as normal, abnormal clinically significant or abnormal not clinically significant
Time Frame: From ICF through 100 days after the last dose of study treatment
|
ECGs results will be summarized and changes from baseline provided
|
From ICF through 100 days after the last dose of study treatment
|
Safety of MILs™ - NSCLC alone and in combination with nivolumab with or without tadalafil by physical examination with abnormalities reported as adverse events
Time Frame: From ICF through 100 days after the last dose of study treatment
|
Physical examinations will be performed by the Investigators and any new clinically significant or changes in medical conditions will be reported as adverse events
|
From ICF through 100 days after the last dose of study treatment
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 15, 2019
Primary Completion (Actual)
October 28, 2021
Study Completion (Actual)
November 30, 2021
Study Registration Dates
First Submitted
August 16, 2019
First Submitted That Met QC Criteria
August 23, 2019
First Posted (Actual)
August 28, 2019
Study Record Updates
Last Update Posted (Actual)
August 2, 2022
Last Update Submitted That Met QC Criteria
July 28, 2022
Last Verified
July 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Respiratory Tract Diseases
- Lung Diseases
- Neoplasms by Site
- Respiratory Tract Neoplasms
- Thoracic Neoplasms
- Carcinoma, Bronchogenic
- Bronchial Neoplasms
- Neoplasms
- Lung Neoplasms
- Carcinoma, Non-Small-Cell Lung
- Molecular Mechanisms of Pharmacological Action
- Vasodilator Agents
- Urological Agents
- Enzyme Inhibitors
- Antineoplastic Agents
- Antineoplastic Agents, Immunological
- Immune Checkpoint Inhibitors
- Phosphodiesterase Inhibitors
- Phosphodiesterase 5 Inhibitors
- Nivolumab
- Tadalafil
Other Study ID Numbers
- CLN-P18001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Yes
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on NSCLC
-
Shanghai Henlius BiotechNot yet recruiting
-
The Netherlands Cancer InstituteEnrolling by invitation
-
Centre Oscar LambretUniversity Hospital, LilleTerminated
-
Suzhou Zelgen Biopharmaceuticals Co.,LtdCompleted
-
Bio-Thera SolutionsCompleted
-
Xinqiao Hospital of ChongqingCompleted
-
Seoul St. Mary's HospitalBoehringer IngelheimActive, not recruiting
-
Taipei Veterans General Hospital, TaiwanNational Taiwan University Hospital; China Medical University Hospital; Tri-Service... and other collaboratorsUnknown
-
AstraZenecaCompletedNSCLCSweden, Bulgaria, Mexico, Russian Federation, Turkey, United Kingdom, Philippines, Malaysia, Germany, Hungary, Latvia, Lithuania, Poland, Romania, Netherlands, Norway, Argentina, Australia, Canada, Slovakia, Greece, Taiwan, Thailand, ... and more
Clinical Trials on MILs™ - NSCLC
-
Fox Chase Cancer CenterWindMIL TherapeuticsWithdrawn
-
Ajou University School of MedicineCompletedOral Surgery | Maxillofacial Surgery
-
University Hospital, RouenCompletedNon Small Cell Lung CancerFrance
-
Sidney Kimmel Comprehensive Cancer Center at Johns...National Institutes of Health (NIH)Active, not recruitingHematologic Malignancies | Graft-Versus-Host DiseaseUnited States
-
Maastricht UniversityUniversity of California, San Francisco; Centre Hospitalier Universitaire de... and other collaboratorsUnknownDetection | SegmentationNetherlands
-
Gruppo Italiano Malattie EMatologiche dell'AdultoRecruitingChronic Lymphocytic Leukemia | Refractory Leukemia | Relapse LeukemiaItaly
-
AVAX TechnologiesTerminatedNon-Small Cell Lung Cancer - Completely ResectableUnited States
-
Goethe UniversityUniversity Hospital Schleswig-HolsteinRecruiting
-
Ethicon Endo-Surgery (Europe) GmbHCompleted
-
National Taiwan University HospitalUnknown