Status:
TERMINATED
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
Lead Sponsor:
WindMIL Therapeutics
Collaborating Sponsors:
Bristol-Myers Squibb
Conditions:
Non Small Cell Lung Cancer
Lung Cancer
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
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 ...
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...
Eligibility Criteria
Inclusion
- 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
- 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.
Key Trial Info
Start Date :
October 15 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 30 2021
Estimated Enrollment :
19 Patients enrolled
Trial Details
Trial ID
NCT04069936
Start Date
October 15 2019
End Date
November 30 2021
Last Update
August 2 2022
Active Locations (10)
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1
City of Hope
Duarte, California, United States, 91010
2
University of California - Los Angeles
Los Angeles, California, United States, 90095
3
Moffitt Cancer Center
Tampa, Florida, United States, 33612
4
Emory University
Atlanta, Georgia, United States, 30322