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Trial record 1 of 1 for:    NCT04683250
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Study of RET Inhibitor TAS0953/HM06 in Patients With Advanced Solid Tumors With RET Gene Abnormalities ((MARGARET))

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04683250
Recruitment Status : Recruiting
First Posted : December 24, 2020
Last Update Posted : March 3, 2023
Sponsor:
Collaborator:
ICON Clinical Research
Information provided by (Responsible Party):
Helsinn Healthcare SA

Study Description
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Brief Summary:
Phase 1 and 2 trial to study the safety, pharmacokinetics, and efficacy of TAS0953/HM06 in patients with advanced solid tumors with RET gene abnormalities. Phase 1 aims to determine the Maximum Tolerated Dose (MTD) and identify the Recommended Phase 2 Dose (RP2D) to be used in phase 2.

Condition or disease Intervention/treatment Phase
RET-altered Non Small Cell Lung Cancer RET-altered Solid Tumors Drug: TAS0953/HM06 Phase 1 Phase 2

Study Design
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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 202 participants
Allocation: Non-Randomized
Intervention Model: Sequential Assignment
Intervention Model Description: Dose escalation phase followed by a dose expansion phase (Phase 1), then followed by a Phase 2 at the recommended dose
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Phase I/II Study of the Selective RET Inhibitor TAS0953/HM06 in Patients With Advanced Solid Tumors With RET Gene Abnormalities
Actual Study Start Date : December 16, 2020
Estimated Primary Completion Date : March 2025
Estimated Study Completion Date : September 2025

Resource links provided by the National Library of Medicine


Arms and Interventions
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Arm Intervention/treatment
Experimental: TAS0953/HM06 Phase 1
Dose escalation and dose expansion until recommended Phase 2 dose determined
 Drug: TAS0953/HM06
Phase 1: oral, starting dose 20mg twice a day, until recommended phase 2 dose, continuous daily dosing, cycles lasting 21 days
Experimental: TAS0953/HM06 Phase 2
Treatment phase at recommended Phase 2 dose in three different populations
 Drug: TAS0953/HM06
Phase 2: oral, recommended dose twice a day, continuous daily dosing, cycles lasting 21 days


Outcome Measures
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Primary Outcome Measures :
  1. Phase 1 (dose-escalation): Maximum Tolerated Dose (MTD) [ Time Frame: At the end of Cycle 1 (each cycle is 21 days) ]
    Incidence rate and category of dose limiting toxicities (DLTs)

  2. Phase 1 (dose-expansion): Recommended Phase 2 dose (RP2D) [ Time Frame: At the end of Cycle 1 (each cycle is 21 days), and at the end of every subsequent cycle (each cycle is 21 days) for approximately 10 months (or earlier if patient discontinues the study) ]
  3. Phase 2: Objective Response Rate (ORR) by independent data monitoring committee (IDMC) [ Time Frame: Approximately every 6 weeks for 6 months, then every 9 weeks during treatment, 7 days after the last dose, and every 3 months after the last dose (up to an average of 2 years) in patients without progressive disease. ]
    Proportion of patients with confirmed complete response (CR) and or partial response (PR) according to RECIST 1.1 as assessed by IDMC


Secondary Outcome Measures :
  1. Phase 1 (dose expansion): Objective Response Rate (ORR) by IDMC [ Time Frame: Approximately every 6 weeks for 6 months, then every 9 weeks during treatment, 7 days after the last dose, and every 3 months after the last dose (up to an average of 2 years) in patients without progressive disease ]
    Proportion of patients with confirmed complete response (CR) and or partial response (PR) according to RECIST 1.1 as assessed by IDMC

  2. Phase 2: ORR by Investigator [ Time Frame: Approximately every 6 weeks for 6 months, then every 9 weeks during treatment, 7 days after the last dose, and every 3 months after the last dose (up to an average of 2 years) in patients without progressive disease ]
    Proportion of patients with confirmed complete response (CR) and or partial response (PR) according to RECIST 1.1 as assessed by Investigator

  3. Phase 2: Disease Control Rate (DCR) [ Time Frame: Approximately every 6 weeks for 6 months, then every 9 weeks during treatment, 7 days after the last dose, and every 3 months after the last dose (up to an average of 2 years) in patients without progressive disease ]
    Proportion of patients with confirmed complete response (CR), partial response (PR) and Stable Disease according to RECIST 1.1 as assessed by Investigator

  4. Phase 2: Time to Tumor Response (TTR) [ Time Frame: From date of randomization until the date of first documentation of objective tumor response, assessed up to an average of 2 years. ]
    Time from first dose to first documentation of objective tumor response (CR or PR)

  5. Phase 2: Progression Free Survival (PFS) [ Time Frame: From date of randomization until the date of first documented progression or death due to any cause, whichever occurs first, assessed up to an average of 2 years. ]
    Time from first dose to first documentation of objective disease progression or to death due to any cause, whichever occurs first

  6. Phase 2: Time to Progression (TTP) [ Time Frame: From date of randomization until the date of first documented progression, assessed up to an average of 2 years ]
    Time from first dose to objective tumor progression

  7. Phase 2: Duration of Response (DOR) [ Time Frame: From first documentation of objective tumor response (CR or PR) until the date of first documented progression or death due to any causes, whichever occurs first, assessed up to an average of 2 years ]
    Time from first documentation of tumor response (CR + PR) to disease progression or death due any cause whichever occurs first

  8. Phase 2: Overall Survival (OS) [ Time Frame: From date of randomization until the date of death due to any cause, assessed up to an average of 2 years ]
    Time from first dose to date of death due to any cause

  9. Phase 2: Central Nervous System (CNS) ORR (C-ORR) [ Time Frame: Approximately every 6 weeks for 6 months, then every 9 weeks during treatment, 7 days after the last dose, and every 3 months after the last dose (up to an average of 2 years) in patients without progressive disease ]
    Rate of confirmed CR and PR relative to patients with brain lesions at study entry

  10. Phase 2: Central Nervous System DOR (C-DOR) [ Time Frame: From first documentation of objective tumor response (CR or PR) until the date of first documented progression or death due to any causes, whichever occurs first, assessed up to an average of 2 years ]
    Time from documentation of intracranial tumor response to disease progression or death due to any cause whichever occurs first

  11. Phase 2: Time to CNS progression [ Time Frame: From date of randomization until the date of first documented progression, assessed up to an average of 2 years ]
    Time from the first dose to the first radiological evidence of CNS disease progression

  12. Phase 1 (dose-escalation): Area under the plasma concentration versus time curve from time 0 to 12 hours (AUC0-12) [ Time Frame: Day -1 of Cycle 1 (each cycle is 21 days) ]
  13. Phase 1 (dose-escalation): AUC0-24 [ Time Frame: Day -1 of Cycle 1 (each cycle is 21 days) ]
  14. Phase 1 (dose-escalation): AUC0-infinity [ Time Frame: Day -1 of Cycle 1 (each cycle is 21 days) ]
  15. Phase 1 (dose-escalation): AUC0-12 at steady state [ Time Frame: Day 15 of Cycle 1 (each cycle is 21 days) ]
  16. Phase 1 (dose-escalation): Maximum drug concentration (Cmax) [ Time Frame: Day -1 and Day 15 of Cycle 1 (each cycle is 21 days) ]
  17. Phase 1 (dose-escalation): Trough drug concentration at 12 hours (Ctrough) [ Time Frame: Day -1 and Day 15 of Cycle 1 (each cycle is 21 days) ]
  18. Phase 1 (dose-escalation): Time to maximum plasma concentration (tmax) [ Time Frame: Day -1 and Day 15 of Cycle 1 (each cycle is 21 days) ]
  19. Phase 1 (dose-escalation): Terminal half-life (t1/2) [ Time Frame: Day -1 and Day 15 of Cycle 1 (each cycle is 21 days) ]
  20. Phase 1 (dose-escalation): Accumulation factor based on Cmax (Rmax) [ Time Frame: Day 15 of Cycle 1 (each cycle is 21 days) ]
  21. Phase 1 (dose-escalation): Accumulation factor based on Ctrough (Rmin) [ Time Frame: Day 15 of Cycle 1 (each cycle is 21 days) ]
  22. Phase 1 (dose-escalation): Terminal rate constant (lambda_z) [ Time Frame: Day -1 and Day 15 of Cycle 1 (each cycle is 21 days) ]
  23. Phase 1 (dose-escalation): Volume of Distribution (Vz/F) [ Time Frame: Day -1 and Day 15 of Cycle 1 (each cycle is 21 days) ]
  24. Phase 1 (dose-escalation): Systemic clearance (CL/F) [ Time Frame: Day -1 and Day 15 of Cycle 1 (each cycle is 21 days) ]
  25. Phase 1 (dose-escalation): Amount excreted in 0-24 hour urine (Ae0-24) [ Time Frame: Day -1 of Cycle 1 (each cycle is 21 days) ]
  26. Phase 1 (dose-escalation): Renal Clearance (CL_R) [ Time Frame: Day -1 of Cycle 1 (each cycle is 21 days) ]
  27. Phase 1 (dose-expansion): AUC0-12 at steady state [ Time Frame: Day 8 and Day 15 of Cycle 1 (each cycle is 21 days) ]
  28. Phase 1 (dose-expansion): Maximum drug concentration (Cmax) [ Time Frame: Day 8 and Day 15 of Cycle 1 (each cycle is 21 days) ]
  29. Phase 1 (dose-expansion): Trough drug concentration at 12 hours (Ctrough) [ Time Frame: Day 8 and Day 15 of Cycle 1 (each cycle is 21 days) ]
  30. Phase 1 (dose-expansion): Time to maximum plasma concentration (tmax) [ Time Frame: Day 8 and Day 15 of Cycle 1 (each cycle is 21 days) ]
  31. Phase 1 (dose-expansion): Terminal rate constant (lambda_z) [ Time Frame: Day 8 and Day 15 of Cycle 1 (each cycle is 21 days) ]
  32. Phase 1 (dose-expansion): Terminal half-life (t1/2) [ Time Frame: Day 8 and Day 15 of Cycle 1 (each cycle is 21 days) ]
  33. Phase 2 Population PK: Typical value of absorption rate constant (Ka) [ Time Frame: Day 15 of Cycle 1 (each cycle is 21 days) ]
  34. Phase 2 Population PK: Typical value of CL/F [ Time Frame: Day 15 of Cycle 1 (each cycle is 21 days) ]
  35. Phase 2 Population PK: Typical value of volume of distribution (V/F) [ Time Frame: Day 15 of Cycle 1 (each cycle is 21 days) ]
  36. Phase 1: Incidence of abnormal electrocardiograms (ECG QT interval). QT will be corrected for heart rate (QTc) using Fridericia's formula (QTcF). [ Time Frame: On Day 1, Day 8 (only in dose escalation), Day 15 in cycle 1, Day 1 of any subsequent cycles (each cycle is 21 days) during treatment, for approximately 10 months (or earlier if the patient discontinues from the study), and 7 days after last dose ]
  37. Phase 1: Incidence of treatment-emergent adverse events (TEAEs) [ Time Frame: From the time of informed consent, for approximately 10 months (or earlier if the patient discontinues from the study), and through Safety Follow-up (28 days after the last dose) ]
  38. Phase 1: Incidence of serious adverse events (SAEs) [ Time Frame: From the time of informed consent, for approximately 10 months (or earlier if the patient discontinues from the study), and through Safety Follow-up (28 days after the last dose) ]
  39. Phase 2: Incidence of abnormal electrocardiograms (ECG QT interval). QT will be corrected for heart rate (QTc) using Fridericia's formula (QTcF). [ Time Frame: On Day 1 and Day 15 in cycle 1, Day 1 of any subsequent cycles (each cycle is 21 days) during treatment, for approximately 2 years (or earlier if the patient discontinues from the study), and 7 days after last dose ]
  40. Phase 2: Incidence of treatment-emergent adverse events (TEAEs) [ Time Frame: From the time of informed consent for approximately 2 years (or earlier if the patient discontinues from the study), and through Safety Follow-up (28 days after the last dose) ]
  41. Phase 2: Incidence of serious adverse events (SAEs) [ Time Frame: From the time of informed consent for approximately 2 years (or earlier if the patient discontinues from the study), and through Safety Follow-up (28 days after the last dose) ]

Eligibility Criteria
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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:

Phase I - Common inclusion criteria for Dose-Escalation / Dose-Expansion:

  • Eastern Cooperative Oncology Group (ECOG) performance score of 0 or 1
  • Available RET-gene abnormalities determined on tissue or liquid biopsy
  • Documented progression of disease following existing therapies deemed by the Investigator to have demonstrated clinical benefit or unable to receive such therapies.
  • Adequate hematopoietic, hepatic and renal function

Phase I Dose-Escalation - Specific inclusion criteria:

  • Advanced solid tumors
  • Measurable and/or non-measurable disease as determined by RECIST 1.1
  • If patient has brain and/or leptomeningeal metastases, (s)he should be asymptomatic.

Phase I Dose-Expansion - Specific inclusion criteria:

  • Locally advanced or metastatic non small cell lung cancer (NSCLC) patients with primary RET gene fusion and prior exposure to RET selective inhibitors
  • Measurable disease as determined by RECIST 1.1

  • If patient has brain and/or leptomeningeal metastases,(s)he should have:

    • asymptomatic untreated brain/leptomeningeal metastases off steroids and anticonvulsant for at least 7 days or
    • asymptomatic brain metastases already treated with local therapy and be clinically stable on steroids and anticonvulsant for at least 7 days before study drug administration.

Phase II :

  • Available RET-gene abnormalities determined on tissue or liquid biopsy

  • Locally advanced or metastatic:

    • NSCLC patients with primary RET gene fusion and prior exposure to RET selective inhibitors;
    • NSCLC patients with RET gene fusion and without prior exposure to RET selective inhibitors
    • patients with advanced solid tumors that harbour RET gene abnormalities (other than NSCLC patients with primary RET gene fusions) and has failed all the available therapeutic options
  • Eastern Cooperative Oncology Group (ECOG) performance score of 0-2
  • Measurable disease as determined by RECIST 1.1

  • If patient has brain and/or leptomeningeal metastases,(s)he should have:

    • asymptomatic untreated brain/leptomeningeal metastases off steroids and anticonvulsant for at least 7 days or
    • asymptomatic brain metastases already treated with local therapy and be clinically stable on steroids and anticonvulsant for at least 7 days before study drug administration.
  • Adequate hematopoietic, hepatic and renal function

Exclusion Criteria:

Common exclusion criteria for Phase 1 and Phase 2

  • Investigational agents or anticancer therapy within 5 half-lives prior to the first dose of study drug
  • Major surgery (excluding placement of vascular access) within 4 weeks prior to the first dose of study drug or planned major surgery during the course of study treatment.
  • Whole Brain Radiotherapy within 14 days or other palliative radiotherapy within 7 days prior to the first dose of study drug, or persisting side effects of such therapy, in the opinion of the Investigator.
  • Clinically significant, uncontrolled, cardiovascular disease including myocardial infarction within 3 months prior to Day 1 of Cycle 1, unstable angina pectoris, significant valvular or pericardial disease, history of ventricular tachycardia, symptomatic Congestive Heart Failure (CHF) New York Heart Association (NYHA) class III-IV, and severe uncontrolled arterial hypertension, according to the Investigator's opinion.
  • QT interval corrected using Fridericia's formula (QTcF) >470 msec; personal or family history of prolonged QT syndrome or history of Torsades de pointes (TdP). History of risk factors for TdP
  • Treatment with strong CYP3A4 inhibitors within 1 week prior to the first dose of study drug or strong CYP3A4 inducers within 3 weeks prior to the first dose of study drug.

Phase I Dose-Expansion - and Phase II specific exclusion criteria:

  • Presence of known EGFR, KRAS, ALK, HER2, ROS1, BRAF and METex14 activating mutations.
Contacts and Locations
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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): NCT04683250


Contacts
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Contact: Michael Karl +49 8709 943 761 Michael.Karl@iconplc.com

Locations
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United States, California
Chao Family Comprehensive Cancer Center Recruiting
Orange, California, United States, 92868-3298
Contact: Sai-Hong Ignatius Ou, MD PhD       ignatius.ou@uci.edu   
Stanford Cancer Center Recruiting
Stanford, California, United States, 94305-5826
Contact: Heather Ann Wakelee, MD       hwakelee@stanford.edu   
United States, Massachusetts
Massachusetts General Hospital Recruiting
Boston, Massachusetts, United States, 02114
Contact: Justin Gainor, MD    617-724-4000      
United States, Michigan
Henry Ford Hospital Recruiting
Detroit, Michigan, United States, 48202
Contact: Shirish Madhav Gadgeel, MD       sgadgee1@hfhs.org   
START Midwest - Cancer & Hematology Centers of Western Michigan Recruiting
Grand Rapids, Michigan, United States, 49546
Contact: Nehal Lakani, MD       nehal.lakhani@startmidwest.com   
United States, New York
Laura and Isaac Perlmutter Cancer Center at NYU Langone Health Recruiting
New York, New York, United States, 10016
Contact: Vamsidhar Velcheti, MD    212-731-5662      
Memorial Sloan Kettering Cancer Center Recruiting
New York, New York, United States, 10065
Contact: Alexander Dela Cruz Drilon, MD    833-401-5560      
United States, Tennessee
The Sarah Cannon Research Institute/Tennessee Oncology Recruiting
Nashville, Tennessee, United States, 37203
Contact: Melissa Johnson, MD       mjohnson@tnonc.com   
United States, Texas
The University of Texas M. D. Anderson Cancer Center Recruiting
Houston, Texas, United States, 77030-4009
Contact: Vivek Subbiah, MD       vsubbiah@mdanderson.org   
Japan
National Cancer Center Hospital East Recruiting
Kashiwa-shi, Chiba, Japan
Contact: Kiyotaka Yoh, MD       kyoh@east.ncc.go.jp   
National Cancer Center Hospital Recruiting
Chuo-ku, Tokyo, Japan, 104-0045
Contact: Yuki Shinno, MD         
The Cancer Institute Hospital of JFCR Recruiting
Koto-ku, Tokyo, Japan, 135-8550
Contact: Shunji Takahashi, MD         
Sponsors and Collaborators
Helsinn Healthcare SA
ICON Clinical Research
More Information
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Responsible Party: Helsinn Healthcare SA
ClinicalTrials.gov Identifier: NCT04683250    
Other Study ID Numbers: HM06-19-26
First Posted: December 24, 2020    Key Record Dates
Last Update Posted: March 3, 2023
Last Verified: March 2023
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Carcinoma, Non-Small-Cell Lung
Congenital Abnormalities
Neoplasms
Carcinoma, Bronchogenic
Bronchial Neoplasms
Lung Neoplasms
 Respiratory Tract Neoplasms
Thoracic Neoplasms
Neoplasms by Site
Lung Diseases
Respiratory Tract Diseases