Ponatinib in Advanced or Metastatic Medullary Thyroid Cancer
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|ClinicalTrials.gov Identifier: NCT03838692|
Recruitment Status : Withdrawn (Closed by sponsor)
First Posted : February 12, 2019
Last Update Posted : October 13, 2021
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|Condition or disease||Intervention/treatment||Phase|
|Medullary Thyroid Cancer||Drug: Ponatinib||Phase 2|
Ponatinib is an investigational agent that blocks abnormal cancer proteins and therefore harms cancer cells. It was recently approved by the Food and Drug Administration for leukemia treatment, but is not approved for medullary thyroid cancer treatment. Early studies, however, have shown that medullary thyroid tumors respond to ponatinib. These studies were done in the laboratory and not performed on humans. This is a study designed for patients with medullary thyroid cancer. Treatment will consist of a drug called ponatinib which is a pill that taken once each day and continue throughout the duration of the study. The purpose of the study is to:
- Determine if this treatment will be effective in decreasing the amount of cancer and, if it does, to determine how long the response will last.
- Determine the side effects that may occur with this treatment.
- To analyze genetic mutations in tumors to help us understand how tumors grow and how these drugs interact with the mechanisms within the tumor.
Ponatinib has been given to many patients with leukemia and is now approved by the United States Food and Drug Administration for treatment of certain types of leukemia. This study will seek to determine if ponatinib can bring benefit to patients with medullary thyroid cancer.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||0 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||A Study of Ponatinib in Advanced or Metastatic Medullary Thyroid Cancer (MTC)|
|Actual Study Start Date :||July 26, 2019|
|Actual Primary Completion Date :||June 14, 2021|
|Actual Study Completion Date :||June 14, 2021|
Experimental: Ponatinib Arm
Ponatinib tablets will be taken by mouth, continuously, once daily at a dose of 30 mg. A cycle of ponatinib is defined as 28 consecutive days starting with the first day of the treatment cycle. Treatment can be taken with water, with or without food, at approximately the same time each day.
A daily oral dose at 30 mg.
Other Name: ICLUSIG
- Objective Response Rate (ORR) [ Time Frame: 24 months ]ORR is defined as the proportion of the subjects in the analysis population who have a complete response (CR) or partial response (PR). Responses are based on assessments per RECIST.
- Progression-Free Survival (PFS) [ Time Frame: 24 months ]PFS is defined as the time from the first day of trial treatment to the first documented disease progression per the Kaplan-Meier curve.
- Total Number of Adverse Reactions [ Time Frame: 24 months ]Testing safety and toxicity assessed using CTCAE criteria
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.
|Ages Eligible for Study:||18 Years and older (Adult, Older Adult)|
|Sexes Eligible for Study:||All|
|Accepts Healthy Volunteers:||No|
- Diagnosis of localized or metastatic unresectable MTC.
- Measurable disease, defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded for non-nodal lesions and short axis for nodal lesions) as ≥20 mm with conventional techniques or as ≥10 mm with spiral computerized tomography (CT) scan.
- The last dose of previous therapy targeting RET kinase must be given at least 4 weeks - Previous treatment with cytotoxic chemotherapy, immunotherapy, or radiotherapy are permitted, if the last dose was given at least 4 weeks prior to the first dose of ponatinib
- Patient must have failed (progressed on or been intolerant of) prior treatment with cabozantinib or vandetanib.
- Age ≥18 years old
- Eastern Cooperative Oncology Group (ECOG) performance status ≤2
- Normal organ and marrow function as defined below:
Negative pregnancy test for women of childbearing potential or male patients, even if surgically sterilized (i.e., status post-vasectomy), who:
- Agree to practice effective barrier contraception during the entire study treatment period and through 4 months after the last dose of study drug, or
- Agree to completely abstain from heterosexual intercourse
- Normal QT interval corrected on screening electrocardiogram (ECG) evaluation, defined as the corrected QT interval by Fredericia (QTcF) of ≤450 ms.
- Ability to understand and the willingness to sign a written informed consent document and follow the guidelines of the clinical protocol including visits for treatment and follow up
- Life expectancy of greater than 12 weeks
- Available archival tissue or willingness to undergo fresh biopsy if no archival tissue is available.
- Patients who are receiving any other investigational agent.
- Patients with brain metastases or spinal cord compression unless they completed radiation therapy ≥4 weeks prior to the first dose of ponatinib and are stable without steroids or anti-convulsant therapy for ≥10 days.
- Patients who cannot discontinue medications that are known to be associated with Torsades de Pointes. These medications are listed in Attachment 3
- Uncontrolled hypertension (systolic blood pressure >150 or diastolic blood pressure >100
- Significant or active cardiovascular disease within 6 months prior to enrollment
- A history of pancreatitis or alcohol abuse
- Uncontrolled hypertriglyceridemia (>450 mg/dL)
- Major surgery (with the exception of minor surgical procedures, such as catheter placement or tumor biopsy) within 28 days prior to the first dose of ponatinib
- Ongoing or active infection including known history of human immunodeficiency virus (HIV), hepatitis B virus (HBV), or hepatitis C (HCV). Testing for these viruses is not required in the absence of a history of infection.
- Suffer from any condition or illness that, in the opinion of the investigator, would compromise patient safety or interfere with the evaluation of the safety of the study drug
- Evidence of a bleeding diathesis that cannot be corrected with standard therapy or factor replacement
- Presence of another primary malignancy within the past 2 years (except for non-melanoma skin cancer or cervical cancer in situ. Prior prostate cancer is also permitted if prostate-specific antigen (PSA) is now undetectable)
- Pregnant or lactating
- History of allergic reactions attributed to compounds of similar chemical or biologic composition to investigational agent
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): NCT03838692
|Principal Investigator:||Antonio Fojo, MD||Columbia University|
|Responsible Party:||Antonio Fojo, Assistant Professor of Medicine at the Columbia University Medical, Columbia University|
|Other Study ID Numbers:||
|First Posted:||February 12, 2019 Key Record Dates|
|Last Update Posted:||October 13, 2021|
|Last Verified:||October 2021|
|Individual Participant Data (IPD) Sharing Statement:|
|Plan to Share IPD:||No|
|Studies a U.S. FDA-regulated Drug Product:||Yes|
|Studies a U.S. FDA-regulated Device Product:||No|
Endocrine Gland Neoplasms
Neoplasms by Site
Head and Neck Neoplasms
Neoplasms, Germ Cell and Embryonal
Neoplasms by Histologic Type
Neoplasms, Glandular and Epithelial
Neoplasms, Nerve Tissue
Endocrine System Diseases
Protein Kinase Inhibitors
Molecular Mechanisms of Pharmacological Action