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Trial record 1 of 1 for:    TAK-981-1502
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A Study of TAK-981 Given With Pembrolizumab in Participants With Select Advanced or Metastatic Solid Tumors

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ClinicalTrials.gov Identifier: NCT04381650
Recruitment Status : Recruiting
First Posted : May 11, 2020
Last Update Posted : February 1, 2023
Sponsor:
Collaborator:
Takeda Development Center Americas, Inc.
Information provided by (Responsible Party):
Takeda

Brief Summary:

TAK-981 is being tested in combination with pembrolizumab to treat participants who have select advanced or metastatic solid tumors.

The study aims are to evaluate the safety, tolerability, and preliminary efficacy of TAK-981 in combination with pembrolizumab.

Participants will be on this combination treatment for 21-day cycles. They will continue with this treatment for up to 24 months or until participants meet any discontinuation criteria.


Condition or disease Intervention/treatment Phase
Advanced or Metastatic Solid Tumors Drug: TAK-981 Drug: Pembrolizumab Phase 1 Phase 2

Detailed Description:

The drug being tested in this study is called TAK-981. TAK-981 is being tested to treat people who have select advanced or metastatic solid tumors. The study will include a dose escalation phase and a dose expansion phase.

The study will enroll approximately 265 patients, approximately 32 participants in the dose escalation phase 1 and approximately 85 to 233 participants in the 9 cohorts of dose expansion phase 2. Participants will receive escalating doses of TAK-981 and fixed dose of pembrolizumab until recommended Phase 2 dose (RP2D) is determined:

• Dose Escalation: TAK-981 + Pembrolizumab (fixed dose)

Once Phase 2 doses are identified, participants of select advanced or metastatic solid tumors will receive TAK-981 in below defined cohorts in the expansion phase 2:

  • Dose Expansion Phase: Cohort A: Non-squamous Non-small Cell Lung Cancer (NSCLC)
  • Dose Expansion Phase: Cohort B: Cervical Cancer
  • Dose Expansion Phase: Cohort C: Microsatellite Stable Colorectal Cancer (MSS-CRC)
  • Dose Expansion Phase: Cohort D: Cutaneous Melanoma
  • Dose Expansion Phase: Cohort E: Squamous NSCLC
  • Dose Expansion Phase: Cohort F: Small Cell Lung Cancer
  • Dose Expansion Phase: Cohort G: Head and Neck Squamous Cell Carcinoma (HNSCC)
  • Dose Expansion Phase: Cohort H: Microsatellite Instability, High Levels/ Mismatch-repair-deficient Colorectal Cancer (MSI-H/dMMR CRC)

This multi-center trial will be conducted worldwide. The overall time to participate in this study is 48 months. Participants will make multiple visits to the clinic, and progression-free survival follow-up for maximum up to 12 months after last dose of study drug.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 265 participants
Allocation: Non-Randomized
Intervention Model: Sequential Assignment
Intervention Model Description: This study has 2 Phases. Phase 1 is dose escalation phase with sequential drug assignment. Phase 2 is parallel assignment.
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase 1b/2 Study of TAK-981 Plus Pembrolizumab to Evaluate the Safety, Tolerability, and Antitumor Activity of the Combination in Patients With Select Advanced or Metastatic Solid Tumors
Actual Study Start Date : August 17, 2020
Estimated Primary Completion Date : September 30, 2023
Estimated Study Completion Date : September 30, 2023

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Dose Escalation: TAK-981 + Pembrolizumab (Fixed Dose)
Escalating doses of TAK-981 with starting dose of 40 mg, intravenous (IV) infusion, on Days 1, 4, 8 and 11 or Days 1 and 8 or Days 1, 8 and 15 in each 21-day Treatment Cycle and pembrolizumab 200 mg, IV infusion, as a fixed dose every 3 weeks on Day 1 of 21-day Treatment Cycle until RP2D is determined (for a maximum of 24 months).
Drug: TAK-981
TAK-981 IV infusion.

Drug: Pembrolizumab
Pembrolizumab IV infusion.

Experimental: Dose Expansion Phase: Cohort A: Non-squamous NSCLC
TAK-981 as IV infusion in participants with non-squamous non-small cell lung cancer (NSCLC) on Days 1, 4, 8 and 11 or Days 1 and 8 or Days 1, 8 and 15 in each 21-day Treatment Cycle up to disease progression or 24-months and pembrolizumab 200 mg IV infusion as a fixed dose every 3 weeks on Day 1 of 21-day Treatment Cycle for a maximum of 24 months.
Drug: TAK-981
TAK-981 IV infusion.

Drug: Pembrolizumab
Pembrolizumab IV infusion.

Experimental: Dose Expansion Phase: Cohort B: Cervical Cancer
TAK-981 as IV infusion in participants with cervical cancer on Days 1, 4, 8 and 11 or Days 1 and 8 or Days 1, 8 and 15 in each 21-day Treatment Cycle up to disease progression or 24-months and pembrolizumab 200 mg IV infusion as a fixed dose every 3 weeks on Day 1 of 21-day Treatment Cycle for a maximum of 24 months.
Drug: TAK-981
TAK-981 IV infusion.

Drug: Pembrolizumab
Pembrolizumab IV infusion.

Experimental: Dose Expansion Phase: Cohort C: MSS-CRC
TAK-981 as IV infusion in participants with microsatellite stable colorectal cancer (MSS-CRC) on Days 1, 4, 8 and 11 or Days 1 and 8 or Days 1, 8 and 15 in each 21-day Treatment Cycle up to disease progression or 24-months and pembrolizumab 200 mg IV infusion as a fixed dose every 3 weeks on Day 1 of 21-day Treatment Cycle for a maximum of 24 months.
Drug: TAK-981
TAK-981 IV infusion.

Drug: Pembrolizumab
Pembrolizumab IV infusion.

Experimental: Dose Expansion Phase: Cohort D: Cutaneous Melanoma
TAK-981 as IV infusion in participants with Cutaneous melanoma on Days 1, 4, 8 and 11 or Days 1 and 8 or Days 1, 8 and 15 in each 21-day Treatment Cycle up to disease progression or 24-months and pembrolizumab 200 mg IV infusion as a fixed dose every 3 weeks on Day 1 of 21-day Treatment Cycle for a maximum of 24 months.
Drug: TAK-981
TAK-981 IV infusion.

Drug: Pembrolizumab
Pembrolizumab IV infusion.

Experimental: Dose Expansion Phase: Cohort E: Squamous NSCLC
TAK-981 as IV infusion in participants with Squamous non-small cell lung cancer (NSCLC) on Days 1, 4, 8 and 11 or Days 1 and 8 or Days 1, 8 and 15 in each 21-day Treatment Cycle up to disease progression or 24-months and pembrolizumab 200 mg IV infusion as a fixed dose every 3 weeks on Day 1 of 21-day Treatment Cycle for a maximum of 24 months.
Drug: TAK-981
TAK-981 IV infusion.

Drug: Pembrolizumab
Pembrolizumab IV infusion.

Experimental: Dose Expansion Phase: Cohort F: Small Cell Lung Cancer
TAK-981 as IV infusion in participants with Small cell lung cancer on Days 1, 4, 8 and 11 or Days 1 and 8 or Days 1, 8 and 15 in each 21-day Treatment Cycle up to disease progression or 24-months and pembrolizumab 200 mg IV infusion as a fixed dose every 3 weeks on Day 1 of 21-day Treatment Cycle for a maximum of 24 months.
Drug: TAK-981
TAK-981 IV infusion.

Drug: Pembrolizumab
Pembrolizumab IV infusion.

Experimental: Dose Expansion Phase: Cohort G: HNSCC
TAK-981 as IV infusion in participants with head and neck squamous cell carcinoma (HNSCC) on Days 1, 4, 8 and 11 or Days 1 and 8 or Days 1, 8 and 15 in each 21-day Treatment Cycle up to disease progression or 24-months and pembrolizumab 200 mg IV infusion as a fixed dose every 3 weeks on Day 1 of 21-day Treatment Cycle for a maximum of 24 months.
Drug: TAK-981
TAK-981 IV infusion.

Drug: Pembrolizumab
Pembrolizumab IV infusion.

Experimental: Dose Expansion Phase: Cohort H: MSI-H/dMMR CRC
TAK-981 as IV infusion in participants with microsatellite instability, high levels/ mismatch-repair-deficient colorectal cancer (MSI-H/dMMR CRC) on Days 1, 4, 8 and 11 or Days 1 and 8 or Days 1, 8 and 15 in each 21-day Treatment Cycle up to disease progression or 24-months and pembrolizumab 200 mg IV infusion as a fixed dose every 3 weeks on Day 1 of 21-day Treatment Cycle for a maximum of 24 months.
Drug: TAK-981
TAK-981 IV infusion.

Drug: Pembrolizumab
Pembrolizumab IV infusion.




Primary Outcome Measures :
  1. Phase 1: Number of Participants With One or More Treatment Emergent Adverse Events (TEAEs) [ Time Frame: Up to 48 months ]
    An adverse event (AE) is any untoward medical occurrence in a participant administered a medicinal investigational drug. The untoward medical occurrence does not necessarily have to have a causal relationship with treatment. A TEAE is defined as an AE that occurs after administration of first dose of study drug and through 30 days after last dose of study drug or until start of subsequent antineoplastic therapy. AEs will be evaluated according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE), v5.0 except cytokine release syndrome (CRS), will be graded according to American society for transplantation and cellular therapy (ASCST) Consensus Grading for CRS.

  2. Phase 1: Number of Participants With Dose Limiting Toxicities (DLTs) [ Time Frame: Up to Cycle 1 (each cycle is of 21 days) ]
    DLTs will be evaluated according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE), v5.0 except cytokine release syndrome (CRS), will be graded according to American society for transplantation and cellular therapy (ASCST) Consensus Grading for CRS.

  3. Phase 1: Number of Participants With Grade 3 or Higher Treatment Emergent Adverse Events (TEAEs) [ Time Frame: Up to 48 months ]
  4. Phase 1: Number of Participants With One or More Serious Adverse Events (SAEs) [ Time Frame: Up to 48 months ]
    An SAE is any untoward medical occurrence that results in death; is life-threatening; requires inpatient hospitalization or prolongation of present hospitalization; results in persistent or significant disability/incapacity; is a congenital anomaly/birth defect or is a medically important event that may not be immediately life-threatening or result in death or hospitalization, but may jeopardize the participant or may require intervention to prevent one of other outcomes listed in definition above, or involves suspected transmission via a medicinal product of an infectious agent.

  5. Phase 1: Number of Participants with One or More TEAEs Leading to Dose Modifications and Treatment Discontinuation [ Time Frame: Up to 48 months ]
  6. Phase 1: Number of Participants With Clinically Significant Laboratory Values [ Time Frame: Up to 48 months ]
    Laboratory parameters includes parameters of clinical chemistry, hematology, and urinalysis.

  7. Phase 2: Overall Response Rate (ORR) as Assessed by the Investigator According to RECIST, Version 1.1 [ Time Frame: Up to 48 months ]
    ORR is defined as the percentage of participants who achieve Complete Response (CR) and Partial Response (PR) (determined by the investigator) during the study according to Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1.


Secondary Outcome Measures :
  1. Phase 1: Cmax: Maximum Observed Plasma Concentration for TAK-981 [ Time Frame: Cycle 1 (each cycle is 21 days) Days 1 and 8 pre-dose and at multiple timepoints (Up to 24 hours); Days 4 and 11: at the end of infusion; Cycle 2, Days 1 and 8, at the end of infusion and at 2 hours post-dose ]
  2. Phase 1: Tmax: Time to Reach the Maximum Plasma Concentration (Cmax) for TAK-981 [ Time Frame: Cycle 1 (each cycle is 21 days) Days 1 and 8 pre-dose and at multiple timepoints (Up to 24 hours); Days 4 and 11: at the end of infusion; Cycle 2, Days 1 and 8, at the end of infusion and at 2 hours post-dose ]
  3. Phase 1: AUCt: Area Under the Plasma Concentration-time Curve from Time 0 to Time t Over the Dosing Interval for TAK-981 [ Time Frame: Cycle 1 (each cycle is 21 days) Days 1 and 8 pre-dose and at multiple timepoints (Up to 24 hours); Days 4 and 11: at the end of infusion; Cycle 2, Days 1 and 8, at the end of infusion and at 2 hours post-dose ]
  4. Phase 1: AUC∞: Area Under the Plasma Concentration-time Curve from Time 0 to Infinity for TAK-981 [ Time Frame: Cycle 1 (each cycle is 21 days) Days 1 and 8 pre-dose and at multiple timepoints (Up to 24 hours); Days 4 and 11: at the end of infusion; Cycle 2, Days 1 and 8, at the end of infusion and at 2 hours post-dose ]
  5. Phase 1: t1/2z: Terminal Disposition Phase Half-life for TAK-981 [ Time Frame: Cycle 1 (each cycle is 21 days) Days 1 and 8 pre-dose and at multiple timepoints (Up to 24 hours); Days 4 and 11: at the end of infusion; Cycle 2, Days 1 and 8, at the end of infusion and at 2 hours post-dose ]
  6. Phase 1: CL: Total Clearance After Intravenous Administration for TAK-981 [ Time Frame: Cycle 1 (each cycle is 21 days) Days 1 and 8 pre-dose and at multiple timepoints (Up to 24 hours); Days 4 and 11: at the end of infusion; Cycle 2, Days 1 and 8, at the end of infusion and at 2 hours post-dose ]
  7. Phase 1: Vss: Volume of Distribution at Steady State After Intravenous Administration for TAK-981 [ Time Frame: Cycle 1 (each cycle is 21 days) Days 1 and 8 pre-dose and at multiple timepoints (Up to 24 hours); Days 4 and 11: at the end of infusion; Cycle 2, Days 1 and 8, at the end of infusion and at 2 hours post-dose ]
  8. Phases 1 and 2: ORR as Defined by the Investigator According to Modified RECIST, Version 1.1 for Immune-Based Therapeutics (iRECIST) Modification [ Time Frame: Up to 48 months ]
  9. Phases 1 and 2: Disease Control Rate (DCR) [ Time Frame: Up to 48 months ]
    DCR is defined as the percentage of participants who achieve stable disease (SD) or better (CR+PR+SD determined by the investigator) during the study.

  10. Phases 1 and 2: Durable Response Rate (DRR) [ Time Frame: Up to 48 months ]
    DRR is defined as the rate of objective responses (CR + PR) maintained for at least 6 months initiating at any time within 12 months of commencing therapy.

  11. Phases 1 and 2: Duration of Response (DOR) [ Time Frame: Up to 48 months ]
    DOR is defined as a time from the time of first documentation of tumor response to the first recorded occurrence of disease progression (PD) or death from any cause (whichever occurs first), through end of study (up to approximately 48 months).

  12. Phases 1 and 2: Progression-free Survival (PFS) [ Time Frame: Up to 48 months ]
    PFS is defined as time from the date of the first dose administration to the date of first documentation of PD or death due to any cause whichever occurs first, through the end of the study (up to approximately 48 months).

  13. Phases 1 and 2: Time to Response (TTR) [ Time Frame: Up to 48 months ]
    TTR is defined as time from the date of the first dose administration to the date of first documented PR or better (up to approximately 48 months).

  14. Phases 1 and 2: Time to Progression (TTP) [ Time Frame: Up to 48 months ]
    TTP is defined as the from the date of the first dose administration to the date of the first documentation of PD as defined by standard disease criteria.

  15. Phase 2: Overall Survival (OS) [ Time Frame: Up to 48 months ]
    OS is defined as the time from the date of the first dose administration to the date of death. Participants without documentation of death at the time of analysis will be censored at the date last known to be alive.

  16. Phase 1: Percentage of Participants at Each Dose Level Demonstrating Adduct Formation in Blood [ Time Frame: Up to 48 months ]
    TAK-981-small ubiquitin-like modifier (SUMO) adduct formation in blood will be evaluated.

  17. Phase 1: Percent Change in Small Ubiquitin-like Modifier (SUMO) 2/3 Signal With Pre and Post-dose in Blood [ Time Frame: Up to 48 months ]
    SUMO pathway inhibition in blood will be evaluated.

  18. Phase 2: Percentage of Participants With One or More Treatment Emergent Adverse Events (TEAEs) [ Time Frame: Up to 48 months ]
  19. Phase 2: Number of Participants With Grade 3 or Higher Treatment Emergent Adverse Events (TEAEs) [ Time Frame: Up to 48 months ]
  20. Phase 2: Number of Participants with One or More TEAEs Leading to Dose Modifications and Treatment Discontinuation [ Time Frame: Up to 48 months ]


Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Has a histologically or cytologically documented, advanced (metastatic and/or unresectable) cancer as listed below that is incurable: Note: Prior neoadjuvant or adjuvant therapy included in initial treatment may not be considered first- or later-line standard of care treatment unless such treatments were completed less than 12 months prior to the current tumor recurrence.

    A. Non-squamous NSCLC for which prior standard first-line treatment containing an anti-programmed cell death protein 1/programmed cell death protein 1 ligand (PD-1/PD-L1) checkpoint inhibitor (CPI) alone or in combination has failed and that has progressed to no more than 1 prior systemic therapy. In Phase 2, participants with non-squamous NSCLC must have not received more than 1 prior systemic therapy and must not have presented with disease progression during the first 6 months of treatment with first-line CPI/anti-PD-(1/L1)-containing therapy.

    Note: In Phase 1, participants with non-squamous NSCLC and known driver mutations/genomic aberrations (e.g., epidermal growth factor receptor (EGFR), B-Raf proto-oncogene mutation V600E [BRAF V600E], and ROS proto-oncogene 1 [ROS1] sensitizing mutations, neurotrophic receptor tyrosine kinase [NRTK] gene fusions, and anaplastic lymphoma kinase [ALK] rearrangements) must have also shown progressive disease after treatment with a commercially available targeted therapy. In Phase 2, participants with driver mutations are not eligible.

    B. CPI-naive cervical cancer (squamous cell carcinoma, adenosquamous carcinoma or adenocarcinoma of the cervix) participants for whom prior standard first-line treatment has failed and who have received no more than 1 prior systemic line of therapy for recurrent or Stage IVB cervical cancer. Note: The following cervical tumors are not eligible: minimal deviation/adenoma malignum, gastric-type adenocarcinoma, clear-cell carcinoma, and mesonephric carcinoma. Histologic confirmation of the original primary tumor is required via pathology report. Note: First-line treatment must have consisted of platinum-containing doublet. Chemotherapy administered concurrently with primary radiation (e.g., weekly cisplatin) is not counted as a systemic chemotherapy regimen.

    C. CPI-naïve microsatellite stable-colorectal cancer (MSS-CRC) participants for whom prior standard first-line treatment has failed and who have progressed on no more than 3 chemotherapy regimens.

    Note: Participants must have received prior treatment with fluoropyrimidine-, oxaliplatin-, and irinotecan-containing regimens if indicated.

    D. Unresectable Stage III or Stage IV cutaneous melanoma that has not received prior therapy with a CPI in the metastatic setting.

    Note: Participants who have presented with disease relapse after ≥6 months of the last dose of CPI or BRAF-mitogen-activated protein kinase kinase (MEK) inhibitor in the adjuvant setting are eligible.

    E. Squamous NSCLC for which prior standard first-line treatment containing an anti-PD-(1/L1) checkpoint inhibitor alone or in combination has failed. Participant must have not received more than 1 prior systemic therapy and must not have presented with disease progression during the first 6 months of treatment with first-line CPI/anti-PD-(1/L1)-containing therapy.

    F. SCLC that has progressed during or after first-line platinum-based chemotherapy regimen or equivalent if platinum-based therapy is contraindicated.

    G. HNSCC (oral cavity, pharynx, larynx) not amenable to local therapy with curative intent that has progressed:

    • Within 6 months of the last dose of platinum therapy in the adjuvant (i.e., with radiation after surgery) or primary (i.e., with radiation) settings, or
    • On or after 1 prior systemic immune CPI/anti-PD-(1/L1)-containing therapy in the metastatic setting. HNSCC participant must have not received more than 1 prior systemic therapy and must not have presented with disease progression during the first 6 months of treatment with first-line CPI or anti-PD-(1/L1)-containing therapy.

    H. Treatment-naïve MSI-H/dMMR CRC.

  2. Has at least 1 radiologically measurable lesion based on RECIST, Version 1.1. Tumor lesions situated in a previously irradiated area are considered measurable if progression has been demonstrated in such lesions.
  3. Has a performance status of 0 or 1 on the Eastern Cooperative Group Oncology (ECOG) Performance Scale.
  4. Has left ventricular ejection fraction (LVEF) ≥40%; as measured by echocardiogram (ECHO) or multiple-gated acquisition (MUGA) scan.
  5. Has recovered to Grade 1 or baseline from all toxicity associated with previous therapy or have the toxicity established as sequela. Note: Has a neuropathy ≤Grade 2, any grade alopecia, or autoimmune endocrinopathies with stable replacement therapy are permitted.
  6. Demonstrate adequate organ function as described below:

A. Platelet count ≥75.0 × 10^9/L. B. Absolute neutrophil count (ANC) ≥1.0 × 10^9/L. C. Hemoglobin ≥85 g/L (red blood cell [RBC] transfusion allowed ≥14 days before assessment).

D. Calculated creatinine clearance ≥30 mL/min using the Cockcroft-Gault formula.

E. Aspartate aminotransferase (AST, GOT) and alanine aminotransferase (ALT, GPT) ≤3.0 times the upper limit of normal (ULN), <5.0 times the ULN if liver enzyme elevations are due to liver metastases; bilirubin ≤1.5 times the ULN. Participants with Gilbert's syndrome may have a bilirubin level >1.5 times the ULN, per discussion between the investigator and the medical monitor.

Exclusion Criteria:

  1. Received extended field radiotherapy ≤4 weeks before the start of treatment (≤7 days for limited field radiation for palliation outside the chest or brain).
  2. History of uncontrolled brain metastasis (evidence of progression by imaging over a period of 4 weeks and/or neurologic symptoms that have not returned to baseline). Participant with treated brain metastases are allowed provided they are radiologically stable, without evidence of progression for at least 4 weeks by repeat imaging, clinically stable, and without requirement of steroid treatment for at least 14 days prior to first dose of study treatment. Note: For asymptomatic participants, screening brain imaging is not required.
  3. Second malignancy within the previous 3 years, except treated basal cell or localized squamous skin carcinomas, localized prostate cancer, cervical carcinoma in situ, resected colorectal adenomatous polyps, breast cancer in situ, or other malignancy for which the participant is not on active anticancer therapy.
  4. Major surgery ≤14 days from the first dose of study drug and not recovered fully from any complications from surgery.
  5. History of immune-related AEs related to treatment with immune CPIs that required treatment discontinuation.
  6. Receiving or requires the continued use of medications that are known to be strong or moderate inhibitors and inducers of cytochrome P-450 (CYP) 3A4/5 and strong P-glycoprotein (Pgp) inhibitors.
  7. Baseline prolongation of the QT interval corrected using Fridericia's formula (QTcF) (e.g., repeated demonstration of QTcF interval >480 ms, history of congenital long QT syndrome, or torsades de pointes).
  8. Has a history of autoimmune disease requiring systemic immunosuppressive therapy with daily doses of prednisone >10 mg/day or equivalent doses, or any other form of immunosuppressive therapy. Hormone therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency) is not considered an excluded form of systemic treatment of an autoimmune disease.
  9. Has a history of noninfectious pneumonitis that required steroids or a history of interstitial lung disease.
  10. Has an evidence of active, non-infectious pneumonitis.
  11. Has a history of allogeneic tissue or solid organ transplant.
  12. Has an active infection requiring systemic therapy.
  13. Has a known history of human immunodeficiency virus (HIV) infection or any other relevant congenital or acquired immunodeficiency.
  14. Has a known hepatitis B virus surface antigen seropositive or detectable hepatitis C infection viral load. Note: Participants who have positive hepatitis B core antibody or hepatitis B surface antigen antibody can be enrolled but must have an undetectable hepatitis B viral load.
  15. History of any of the following ≤6 months before first dose: congestive heart failure New York Heart Association Grade III or IV, unstable angina, myocardial infarction, unstable symptomatic ischemic heart disease, uncontrolled hypertension despite appropriate medical therapy, ongoing symptomatic cardiac arrhythmias >Grade 2, pulmonary embolism or symptomatic cerebrovascular events, or any other serious cardiac condition (e.g., pericardial effusion or restrictive cardiomyopathy). Chronic atrial fibrillation on stable anticoagulant therapy is allowed.
  16. Psychiatric illness/social circumstances that would limit compliance with study requirements and substantially increase the risk of AEs or has compromised ability to provide written informed consent.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04381650


Contacts
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Contact: Takeda Contact +1-877-825-3327 medinfoUS@takeda.com

Locations
Show Show 65 study locations
Sponsors and Collaborators
Takeda
Takeda Development Center Americas, Inc.
Investigators
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Study Director: Study Director Takeda
Additional Information:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Takeda
ClinicalTrials.gov Identifier: NCT04381650    
Other Study ID Numbers: TAK-981-1502
2020-004325-23 ( EudraCT Number )
jRCT2031210417 ( Registry Identifier: jRCT )
First Posted: May 11, 2020    Key Record Dates
Last Update Posted: February 1, 2023
Last Verified: January 2023
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
Plan Description: Takeda provides access to the de-identified individual participant data (IPD) for eligible studies to aid qualified researchers in addressing legitimate scientific objectives (Takeda's data sharing commitment is available on https://clinicaltrials.takeda.com/takedas-commitment?commitment=5). These IPDs will be provided in a secure research environment following approval of a data sharing request, and under the terms of a data sharing agreement.
Supporting Materials: Study Protocol
Statistical Analysis Plan (SAP)
Informed Consent Form (ICF)
Clinical Study Report (CSR)
Access Criteria: IPD from eligible studies will be shared with qualified researchers according to the criteria and process described on https://vivli.org/ourmember/takeda/. For approved requests, the researchers will be provided access to anonymized data (to respect patient privacy in line with applicable laws and regulations) and with information necessary to address the research objectives under the terms of a data sharing agreement.
URL: https://vivli.org/ourmember/takeda/

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Product Manufactured in and Exported from the U.S.: No
Keywords provided by Takeda:
Drug therapy
Additional relevant MeSH terms:
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Neoplasms
Pembrolizumab
Antineoplastic Agents, Immunological
Antineoplastic Agents