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Trial record 1 of 2 for:    LY3410738
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Study of LY3410738 Administered to Patients With Advanced Solid Tumors With IDH1 Mutations

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ClinicalTrials.gov Identifier: NCT04521686
Recruitment Status : Recruiting
First Posted : August 20, 2020
Last Update Posted : November 23, 2020
Sponsor:
Collaborator:
Eli Lilly and Company
Information provided by (Responsible Party):
Loxo Oncology, Inc.

Brief Summary:
This is an open-label, multicenter Phase 1 study to evaluate safety, tolerability and preliminary efficacy of oral LY3410738 in patients with IDH1 R132-mutant advanced solid tumor types, including but not limited to cholangiocarcinoma, chondrosarcoma, and glioma.

Condition or disease Intervention/treatment Phase
Cholangiocarcinoma Chondrosarcoma Glioma Any Solid Tumor Drug: LY3410738 Phase 1

Detailed Description:

This is an open-label, multicenter Phase 1 study to evaluate safety, tolerability and preliminary efficacy of oral LY3410738 in patients with IDH1 R132-mutant advanced solid tumor types, including but not limited to cholangiocarcinoma, chondrosarcoma, and glioma.

This study includes 2 parts, Phase 1 dose escalation and Phase 1 dose expansion. The Phase 1 dose escalation monotherapy cohort will enroll any eligible patient with IDH1 R132-mutant advanced solid tumor. Once the LY3410738 monotherapy RP2D is established, Phase 1 dose expansion will begin and will include 4 cohorts to further evaluate safety and clinical activity - three cohorts will be administered LY3410738 monotherapy and the fourth cohort wiil administer LY3410738 to patients in combination with gemcitabine and cisplatin.

IDH1 R132 mutations will be identified through standard of care testing as routinely performed at each participating site utilizing material collected prior to patient consent . Molecular assays utilized for enrollment are required to be performed in CLIA, ISO/IEC, CAP, or other similarly certified laboratory. Enrollment of patients with cholangiocarcinoma, chondrosarcoma or glioma may be made based on molecular tests performed in either tumor or blood. Enrollment of patients with other tumor types is limited to testing performed in tumor tissue.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 180 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Study of LY3410738 Administered to Patients With Advanced Solid Tumors With IDH1 Mutations
Actual Study Start Date : October 16, 2020
Estimated Primary Completion Date : February 2023
Estimated Study Completion Date : September 2023


Arm Intervention/treatment
Experimental: LY3410738
Phase 1 dose escalation - Multiple doses of LY3410738 Phase 1 dose expansion - The maximum tolerated dose (MTD)/recommended Phase 2 dose (RP2D)
Drug: LY3410738
Oral LY3410738




Primary Outcome Measures :
  1. Recommended Phase 2 dose (RP2D) [ Time Frame: Up to 24 months ]

Secondary Outcome Measures :
  1. Objective Response Rate [ Time Frame: Up to 24 months ]
  2. Assess the safety and tolerability of LY3410738 when administered alone or in combination with cisplatin plus gemcitabine. [ Time Frame: Up to 24 months ]
  3. To assess the preliminary anti-tumor activity of LY3410738 monotherapy and in combination with cisplatin plus gemcitabine [ Time Frame: Up to 24 months ]
  4. Characterize PK properties of LY3410738 when administered alone or in combination with cisplatin plus gemcitabine. [ Time Frame: Up to 24 months ]
  5. To characterize the pharmacodynamic properties of LY3410738 as expressed by change in 2-HG oncometabolite levels in plasma. [ Time Frame: Up to 24 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.


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

Inclusion Criteria:

  1. Evidence of IDH1 R132 mutation in tumor tissue (any solid tumor) or circulating tumor DNA (cholangiocarcinoma, chondrosarcoma, and glioma) as determined by molecular testing routinely performed at a CLIA, ISO/IEC, CAP, or other similarly certified laboratory.
  2. Availability of an archived tumor tissue sample
  3. Eastern Cooperative Oncology Group (ECOG) 0-1
  4. At least 18 years of age
  5. Adequate organ function
  6. Ability to swallow capsules
  7. Ability to comply with outpatient treatment, laboratory monitoring, and required clinic visits for the duration of study participation
  8. For cholangiocarcinoma patients, must have adequate biliary drainage (per investigator's discretion), with no evidence of ongoing infection.
  9. Willingness of men and women of reproductive potential to observe conventional and effective birth control for the duration of treatment and for 3 months following the last dose of study treatment.

    Monotherapy Dose Escalation:

  10. A locally advanced or metastatic solid tumor, where standard curative or palliative measures are no longer effective or are not considered appropriate or safe in the opinion of the investigator.
  11. Measurable or non-measurable disease as determined by RECIST 1.1 or RANO as appropriate by tumor type.
  12. Prior IDH1 inhibitor treatment is permitted.

    Monotherapy Dose Expansion Cohort 1:

  13. Histologically or cytologically confirmed diagnosis of advanced or metastatic cholangiocarcinoma, following 1 to 2 lines of prior systemic treatment for advanced disease. Prior IDH1 inhibitor treatment is not permitted.
  14. Measurable disease as determined by RECIST 1.1.

    Monotherapy Dose Expansion Cohort 2:

  15. A locally advanced or metastatic solid tumor (except for cholangiocarcinoma), where standard curative or palliative measures are no longer effective or are not considered appropriate or safe in the opinion of the investigator.
  16. Measurable disease as determined by RECIST 1.1 or RANO as appropriate by tumor types.

    Monotherapy Dose Expansion Cohort 3:

  17. A locally advanced or metastatic solid tumor, where standard curative or palliative measures are no longer effective or are not considered appropriate or safe in the opinion of the investigator.
  18. Non-measurable disease only as determined by RECIST 1.1 or RANO as appropriate by tumor type.

    Combination Dose Expansion Cohort 4:

  19. Histologically or cytologically confirmed diagnosis of advanced or metastatic cholangiocarcinoma, not eligible for curative resection.
  20. No prior systemic therapy for advanced or metastatic disease with the following exceptions:

    • Patients who received adjuvant chemotherapy are eligible, if the adjuvant therapy was completed at least 6 months prior to the development of advanced or metastatic disease.
    • Patients who are receiving the first cycle of cisplatin plus gemcitabine as the first line systemic therapy while waiting for results of locally obtained molecule profiling including IDH1 mutational status, are eligible, provided that a radiographic assessment during screening demonstrates the absence of interval disease progression since initiation of chemotherapy treatment, and all other eligibility criteria are met.
  21. Measurable disease as determined by RECIST 1.1.

Exclusion Criteria:

  1. Had an investigational agent or anticancer therapy within 2 weeks; or investigational monoclonal antibody within 4 weeks prior to planned start of LY3410738.
  2. Had major surgery within 4 weeks prior to planned start of LY3410738.
  3. Had radiotherapy with a limited field of radiation for palliation within 7 days of the first dose of study treatment, except for patients receiving whole brain radiotherapy, which must be completed at least 4 weeks prior to the first dose of study treatment.
  4. Patients with cholangiocarcinoma: underwent hepatic radiation, chemoembolization and radiofrequency ablation, radioembolization or other locoregional therapy <4 weeks, have history of hepatic encephalopathy of any grade, have ascites requiring intervention such as diuretics or paracentesis, have ongoing cholangitis, have mixed hepatocellular biliary tract cancer histology
  5. Have active CNS metastases are not eligible. Patients with asymptomatic and treated brain metastases may participate provided that they are stable and are not requiring steroid treatment. Patients with suspected or confirmed leptomeningeal disease are not eligible even if treated.
  6. Have primary CNS tumors are eligible provided that they do not have leptomeningeal disease and are on a stable or decreasing steroid dose for 7 days prior to screening. Patients with evidence of intracranial hemorrhage either by MRI or CT are not eligible
  7. Any unresolved toxicities from prior therapy greater than CTCAE (version 5.0) Grade 2 at the time of starting study treatment except for alopecia.
  8. Have clinically significant, uncontrolled cardiac, cardiovascular disease or history of myocardial infarction within 6 months prior to planned start of study treatment.
  9. Have active uncontrolled systemic bacterial, viral, fungal or parasitic infection (except for fungal nail infection), or other clinically significant active disease process which in the opinion of the investigator and the sponsor makes it undesirable for the patient to participate in the trial. Screening for chronic conditions is not required.
  10. Known active hepatitis B virus (HBV). Note: Controlled (treated) hepatitis will be allowed if they meet the following criteria, antiviral therapy for HBV must be given for at least 1 month prior to first dose of study drug, and HBV viral load must be less than 2000 IU/ml (104 copies/ml) prior to the first dose of study drug. Those on active HBV therapy with viral loads under 2000 IU/ml (104 copies/ml) should stay on the same therapy throughout the study treatment (Appendix E).
  11. Known active hepatitis C virus (HCV). Note: Untreated patients with chronic infection by HCV are allowed on study. In addition, successfully treated patients (defined as sustained virologic response SVR12 or SVR24) are allowed, as long as there is 4 weeks between achieving sustained viral response (SVR12 or SVR24) and starting study drug.
  12. Known human immunodeficiency virus (HIV); excluded due to potential drug-drug interactions between anti-retroviral medications and LY3410738.
  13. Current treatment with certain strong cytochrome P450 3A4 (CYP3A4) inhibitors or inducers (Appendix F) and/or strong P-gp inhibitor (Appendix G).
  14. Treatment with proton pump inhibitor (PPIs) within 7 days of starting LY3410738 (Appendix H). For recommended alternatives, refer to Section 6.4.3.
  15. Clinically significant active malabsorption syndrome or other condition likely to affect gastrointestinal absorption of the study drug.
  16. Active second malignancy unless in remission and with life expectancy > 2 years. Refer to protocol exclusion criteria (Section 4.2) for examples of allowed second malignancies.
  17. Pregnancy, lactation or plan to breastfeeding during the study or within 30 days of the last dose of study intervention.
  18. Patients with known hypersensitivity to any component of LY3410738 or its formulation.

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): NCT04521686


Contacts
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Contact: Patient Advocacy 833-LOXO-IDH clinicaltrials@loxooncology.com

Locations
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United States, Arizona
The University of Arizona Cancer Center Recruiting
Tucson, Arizona, United States, 85724
United States, Indiana
Indiana University SImon Comprehensive Cancer Center Recruiting
Indianapolis, Indiana, United States, 46202
United States, Tennessee
Sarah Cannon Research Institute Recruiting
Nashville, Tennessee, United States, 37203
United States, Texas
The University of Texas MD Anderson Cancer Center Recruiting
Houston, Texas, United States, 77030
South Texas Accelerated Research Therapeutics, LLC Recruiting
San Antonio, Texas, United States, 78229
Japan
National Cancer Center East Recruiting
Kashiwa-shi, Chiba, Japan, 277-8577
National Cancer Center Hospital Recruiting
Tokyo, Japan, 104-0045
Sponsors and Collaborators
Loxo Oncology, Inc.
Eli Lilly and Company
Investigators
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Study Director: Thomas Xu Medical Monitor
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Responsible Party: Loxo Oncology, Inc.
ClinicalTrials.gov Identifier: NCT04521686    
Other Study ID Numbers: LOXO-IDH-20002
2020-002863-77 ( EudraCT Number )
First Posted: August 20, 2020    Key Record Dates
Last Update Posted: November 23, 2020
Last Verified: September 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Loxo Oncology, Inc.:
IDH1
CNS tumor
Cholangiocarcinoma
Chondrosarcoma
Glioma
Glioblastoma
Solid tumor
Primary CNS tumor
Colon cancer
Cancer of the Colon
Colon Neoplasms
Colonic Cancer
Neoplasms, Colonic
Malignant tumor of Breast
Mammary Cancer
Mammary Carcinoma, Human
Mammary Neoplasm, Human
Neoplasms, Breast
Tumors, Breast
Human Mammary Carcinoma
Malignant Neoplasm of Breast
Breast Carcinoma
Breast Tumors
Cancer of the Breast
Breast Neoplasms
Breast Cancer
Thyroid cancer
Prostate cancer
Melanoma
IDH1 R132
Additional relevant MeSH terms:
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Glioma
Cholangiocarcinoma
Chondrosarcoma
Neoplasms
Neoplasms, Neuroepithelial
Neuroectodermal Tumors
Neoplasms, Germ Cell and Embryonal
Neoplasms by Histologic Type
Neoplasms, Glandular and Epithelial
Neoplasms, Nerve Tissue
Adenocarcinoma
Carcinoma
Neoplasms, Connective Tissue
Neoplasms, Connective and Soft Tissue
Sarcoma