NCT04350463 - A Safety and Efficacy Study of CC-90011 in Combination With Nivolumab in Subjects With Advanced Cancers | Crick

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: Subjects must satisfy the following criteria to be enrolled in the study: 1. Subject is ≥ 18 years of age at the time of signing the informed consent form (ICF). 2. Subject with histological or cytological confirmation of extensive stage Small Cell Lung Cancer (ES SCLC) or Stage IIIb or IV squamous Non-Small Cell Lung Cancer (sqNSCLC) 3. Subject has received 1 or 2 prior lines of therapies, defined as: 1. Cohort A (SCLC, Immune Checkpoint Inhibitor naïve): * At least 1 prior treatment including a platinum-based chemotherapy doublet * A minimum of 3 cycles of platinum-based chemotherapy in first line treatment, unless stopped at 2 cycles due to treatment-related toxicity 2. Cohort B (SCLC, ICI progressors): * At least 1 prior first or second line treatment includes an ICI * If treatment includes an ICI as maintenance therapy, at least 1 cycle of ICI in maintenance should have been completed * At least 1 prior treatment including a platinum-based chemotherapy doublet * A minimum of 3 cycles of platinum-based chemotherapy, with or without ICI, in first line treatment, unless stopped at 2 cycles due to treatment-related toxicity * Subject must have progressed during ICI therapy, defined as unequivocal progression on or within 3 months of the last dose of ICI therapy (if no subsequent therapy) 3. Cohort C (sqNSCLC, ICI progressors): * At least 1 prior first or second line treatment includes an ICI * If treatment includes an ICI as maintenance therapy, at least 1 cycle of ICI in maintenance should have been completed * At least 1 prior treatment including a platinum-based chemotherapy doublet * A minimum of 3 cycles of platinum-based chemotherapy, with or without an ICI, in first line treatment, unless stopped at 2 cycles due to treatment-related toxicity * Subject must have progressed during ICI therapy, defined as unequivocal progression on or within 3 months of the last dose of ICI therapy (if no subsequent therapy) 4. Subject has progressed at the last line of therapy. 5. Subject has a measurable disease defined by RECIST v1.1. 6. Subject agrees to provide a tumor biopsy from primary or metastatic site prior to first dose and at a pre-specified timepoint during treatment. Core biopsy is required however, in the event a core biopsy may not otherwise be feasible in the opinion of the treating physician, an endobronchial ultrasound-guided fine needle aspirate \[EBUS-FNA\]) biopsy, using the largest gauge needle, may be performed instead. 7. Subject has ECOG Performance Status of 0 to 1. 8. Subject must have the following laboratory values: 1. Absolute neutrophil count (ANC) ≥ 1.5 x 109/L 2. Hemoglobin (Hgb) ≥ 9 g/dL (one-time blood transfusion is allowed) 3. Platelet (Plt) Count ≥ 150 x 109/L 4. White blood cells (WBC) ≥ 2 x 109L 5. Serum AST/serum glutamic oxaloacetic transaminase (SGOT) or ALT/serum glutamic pyruvic transaminase (SGPT) ≤ 3 x upper limit of normal (ULN) or ≤ 5 x ULN if presence of liver metastases 6. Total serum bilirubin ≤ 1.5 x ULN (≤ 3 x ULN, if Gilbert's syndrome or if indirect bilirubin concentrations are suggestive of extrahepatic source of the elevation) 7. Creatinine clearance (CrCl) ≥ 60 mL/minute based on Cockcroft-Gault or modification of diet in renal disease (MDRD) or ≥ 60 mL/min/1.73 m2 Exclusion Criteria: The presence of any of the following will exclude a subject from enrollment: 1. Subject has not recovered to Grade 2 or lower clinically significant toxicities related to the prior therapy (alopecia excluded). 2. Subject has received prior LSD1 therapies. 3. Subject has a history of severe hypersensitivity reactions to other monoclonal antibodies 4. Subject with symptomatic and untreated or unstable central nervous system (CNS) metastases. 1. Subject has recently been treated with whole brain radiation or stereotactic radiosurgery for CNS metastases must have completed therapy at least 2 weeks prior to Cycle 1 Day 1 and has a follow-up brain computed tomography (CT) or magnetic resonance imaging (MRI) demonstrating either stable or improving metastases 2 or more weeks after completion of radiotherapy. 2. Subject must be asymptomatic and off steroids or on stable dose of steroids for at least 2 weeks (≤ 10 mg daily prednisone or equivalent) prior to first dose. 5. Subject has persistent diarrhea due to a malabsorptive syndrome (such as celiac sprue or inflammatory bowel disease) ≥ NCI CTCAE Grade 2, despite medical management), or any other significant gastrointestinal (GI) disorder that could affect the absorption of the study treatments. 6. Subject with symptomatic or uncontrolled ulcers (gastric or duodenal), particularly those with a history of and/or risk of perforation and GI tract hemorrhages. 7. Subject with any hemorrhage/bleeding event \> NCI CTCAE Grade 2 or haemoptysis \> 1 teaspoon within 4 weeks prior to the first dose. 8. Subject has any of the following cardiovascular criteria: 1. Evidence of acute or ongoing cardiac ischemia 2. Current symptomatic pulmonary embolism 3. Unstable angina pectoris or myocardial infarction ≤ 6 months prior to enrollment 4. Heart failure of New York Heart Association Classification III or IV ≤ 6 months prior to enrollment 5. Persistent or clinically meaningful ventricular arrhythmias prior to enrollment 6. Cerebral vascular accident or transient ischemic attack ≤ 6 months prior to enrollment 7. QT corrected based on Fridericia's equation (QTcF) ≥ 450 milliseconds (msec) on Screening ECG, a baseline prolongation of QTcF interval ≥ 450 msec (NCI CTCAE Grade ≥ 2) 8. A history of additional risk factors for Torsades de pointes (TdP) (eg, heart failure, hypokalemia, family history of Long QT Syndrome) 9. Uncontrolled hypertension (blood pressure ≥ 160/95 mm Hg) 9. Subject has known human immunodeficiency virus (HIV) infection. 10. Subject has known chronic active hepatitis B or C virus (HBV, HCV) infection. 1. Subject who is seropositive due to HBV vaccination is eligible. 2. Subject who has no active viral infection and is under adequate prophylaxis against HBV reactivation is eligible. 11. Subject has any other malignancy within 2 years prior to enrollment, with the exception of adequately treated in-situ bladder cancer, in-situ carcinoma of the cervix, uteri, nonmelanomatous skin cancer, ductal in situ breast carcinoma, thyroid cancer, or early stage prostate cancer (all treatment of which should have been completed 6 months prior to enrollment). 12. Subject has medical conditions requiring systemic treatment with either corticosteroids (\> 10 mg daily prednisone or equivalent) or other immunosuppressive medications within 14 days of enrollment. 1. A brief (≤ 7 days) course of corticosteroids for prophylaxis (eg, contrast dye allergy) or for treatment of nonautoimmune conditions (eg, delayed-type hypersensitivity reaction caused by contact allergen) is permitted. 2. Adrenal replacement steroid doses \> 10 mg daily prednisone or equivalent are permitted in the absence of active autoimmune disease. 3. Topical, ocular, intra-articular, intranasal, and inhalational corticosteroids (with minimal systemic absorption) are permitted. 13. Subject has active autoimmune diseases or history of autoimmune diseases that may relapse. Subjects with the following diseases are allowed to be enrolled after further screening: type I diabetes, hypothyroidism managed with hormone replacement therapy only, skin diseases not requiring systemic treatment (such as vitiligo, psoriasis, or alopecia), or diseases not expected to recur in the absence of external triggering factors. 14. Subject is pregnant or nursing. 15. Subject has a history of persistent skin rash ≥ NCI CTCAE Grade 2 related to prior ICI therapy. 16. Subject has organ transplant history, including allogeneic stem cell transplant. 17. Subject has interstitial lung disease history. 18. Subject has received a live/attenuated vaccine within 30 days of first dose. 19. Subject has previous SARS-CoV-2 infection either suspected or confirmed within 4 weeks prior to screening. 1. Acute symptoms must have resolved and based on Investigator assessment in consultation with the Medical Monitor, there are no sequelae that would place the subject at a higher risk of receiving investigational treatment.

Outcomes

Primary Outcomes

Overall Response Rate

Overall response rate was defined as the percentage of participants in the treated population who had confirmed complete response (CR) or confirmed partial response (PR) as assessed by Investigator review per RECIST v1.1. CR was defined as disappearance of all target lesions and any pathological lymph nodes (whether target or non-target) must have reduction in short axis to \< 10 millimeter (mm). PR was defined as at least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum diameters. Disease progression (PD) is defined as an additional 10% increase in tumor burden with a minimum 5 mm absolute increase from time of initial PD. This includes an increase in the sum of diameters of all target lesions and/or the diameters of new measurable lesions compared to the time of the initial PD.

Time frame: Every 6 weeks post Cycle 1 (each cycle is of 28 days) Day 1 for the first 24 weeks and then every 8 weeks until disease progression, new anticancer therapy, death or withdrawal by participants (up to approximately 33 months)

Secondary Outcomes

Number of Participants With Treatment Emergent Adverse Events by Maximal National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE)

An Adverse Event (AE) is defined as any new untoward medical occurrence or worsening of a preexisting medical condition in a clinical investigation participant administered study treatment and that does not necessarily have a causal relationship with this treatment. Treatment-emergent Adverse Events are defined as any AEs that begin or worsen on or after the start of study drug through 28 days after the last dose of CC-90011 or until 100 days after last dose of nivolumab study treatment. AEs were graded using the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 (Grade 1=mild, Grade 2=Moderate, Grade 3 = Severe, Grade 4 = Life-threatening, Grade 5 = Death).

Time frame: From the start of study drug through 28 days after the last dose of CC-90011 or until 100 days after last dose of Nivolumab (up to 849 days)

Number of Participants With Laboratory Results With CTCAE Toxicity Grade >=3 for Hematology Parameters

Laboratory results were graded using the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 (Grade 3 =Severe, Grade 4 = Life-threatening).

Time frame: Cycle 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 14 and 18 (each cycle is of 28 days)

Number of Participants With Laboratory Results With CTCAE Toxicity Grade >=3 for Chemistry Parameters

Laboratory results were graded using the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 (Grade 3 =Severe, Grade 4 = Life-threatening).

Time frame: Cycle 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 14 and 18 (Each cycle is of 28 days)

Number of Participants Receiving Concomitant Medication

Concomitant medication is defined as medications that were either initiated before the first dose of study drug and continued during the study treatment, or initiated on/after the date of the first dose of study drug and on/before the date of treatment discontinuation.

Time frame: From first dose till treatment discontinuation due to any reason (Up to approximately 107 weeks)

Change From Baseline at End of Treatment in Vital Sign - Weight

Baseline value was defined as the last non-missing value on or before the day that first dose of study drug is administered; if multiple values are present for the same date, the average of these values will be used as the baseline.

Time frame: Baseline and End of Treatment (Up to 107 weeks)

Change From Baseline at End of Treatment in Vital Sign - Diastolic Blood Pressure (DBP) and Systolic Blood Pressure (SBP)

Time frame: Baseline and End of Treatment (Up to 107 weeks)

Change From Baseline at End of Treatment in Vital Sign - Temperature

Time frame: Baseline and End of Treatment (Up to 107 weeks)

Change From Baseline at End of Treatment in Vital Sign - Pulse Rate

Time frame: Baseline and End of Treatment (Up to 107 weeks)

Number of Participants With Post-Baseline Grade Shift in Eastern Cooperative Oncology Group Performance (ECOG) Status

ECOG Scale was used to assess performance status. Grades: 0: Fully active, able to carry on all pre-disease performance without restriction. 1: Restricted in physically strenuous activity but ambulatory, able to carry out work of light nature. 2: Ambulatory, capable of self-care, unable to carry out work activities. Up and about more than 50% waking hours. 3: Capable of limited self-care, confined to bed/chair more than 50% waking hours. 4: Completely disabled. Cannot carry on any self-care. Totally confined to bed/chair. 5: Dead. Baseline value was defined as the last non-missing value on or before the day that first dose of study drug is administered; if multiple values are present for the same date, the average of these values will be used as the baseline.

Time frame: Baseline and up to End of Treatment (107 weeks)

Number of Participants With Treatment-emergent Adverse Events Leading to Dose Reduction of CC-90011

Adverse Event (AE) is defined as any new untoward medical occurrence or worsening of a preexisting medical condition in a clinical investigation participant administered study treatment and that does not necessarily have a causal relationship with this treatment. Treatment-emergent Adverse Events are defined as any AEs that begin or worsen on or after the start of study drug through 28 days after the last dose of CC-90011 or until 100 days after last dose of nivolumab study treatment.

Time frame: From the start of study drug through 28 days after the last dose of CC-90011 or until 100 days after last dose of Nivolumab (up to 849 days)

Number of Participants With Treatment-emergent Adverse Events Leading to Dose Interruption of CC-90011

Time frame: From the start of study drug through 28 days after the last dose of CC-90011 or until 100 days after last dose of Nivolumab (up to 849 days)

Number of Participants With Treatment-emergent Adverse Events Leading to Dose Interruption of Nivolumab

Time frame: From the start of study drug until 100 days after last dose of Nivolumab (up to 849 days)

Duration of Response

Duration of Response was defined as the time from the first occurrence of a confirmed documented response to the time of the first documented tumor progression, as determined by Investigator review per RECIST v1.1, or death from any cause, whichever comes first. CR was defined as disappearance of all target lesions and any pathological lymph nodes (whether target or non-target) must have reduction in short axis to \< 10 millimeter (mm). PR was defined as at least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum diameters. Disease progression (PD) is defined as an additional 10% increase in tumor burden with a minimum 5 mm absolute increase from time of initial PD. This includes an increase in the sum of diameters of all target lesions and/or the diameters of new measurable lesions compared to the time of the initial PD.

Time frame: Every 6 weeks post cycle 1 day 1 (each cycle is of 28 days) for the first 24 weeks and then every 8 weeks until disease progression, new anticancer therapy, death or withdrawal by participant (up to approximately 33 months))

Time to Response

Time to response was defined as the time from the first dose of the study drug to the date of the first confirmed documented response (CR or PR), as assessed by Investigator review per RECIST v1.1. CR was defined as disappearance of all target lesions and any pathological lymph nodes (whether target or non-target) must have reduction in short axis to \< 10 millimeter (mm). PR was defined as at least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum diameters. Disease progression (PD) is defined as an additional 10% increase in tumor burden with a minimum 5 mm absolute increase from time of initial PD. This includes an increase in the sum of diameters of all target lesions and/or the diameters of new measurable lesions compared to the time of the initial PD.

Progression-Free Survival

Progression-Free Survival is the time from first dose of study treatment to the date of the first objectively documented tumor progression as assessed by Investigator review per RECIST v1.1 or death from any cause, whichever occurs first. Disease progression (PD) is defined as an additional 10% increase in tumor burden with a minimum 5 mm absolute increase from time of initial PD. This includes an increase in the sum of diameters of all target lesions and/or the diameters of new measurable lesions compared to the time of the initial PD.

Time to First Subsequent Therapy

Time to First Subsequent Therapy was defined as the time from the first dose of the study drug to the date of the next cancer therapy or death.

Time frame: From the first dose of study drug to the date of next cancer therapy or death due to any cause (up to approximately 33 months)

A Safety and Efficacy Study of CC-90011 in Combination With Nivolumab in Subjects With Advanced Cancers

Overview

Conditions

Interventions

Eligibility

Locations (37)

Outcomes

Primary Outcomes

Secondary Outcomes