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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02048488
Other study ID # PR-20-5006-C
Secondary ID
Status Completed
Phase Phase 1/Phase 2
First received
Last updated
Start date October 2012
Est. completion date June 2018

Study information

Verified date March 2016
Source Tesaro, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

TSR-011 is a potent small molecule inhibitor of tyrosine kinases involved in cancer, including:

1. Anaplastic lymphoma kinase (ALK)

2. The tropomyosin-related kinases TRKA, TRKB, and TRKC

This is a sequential, open-label, non-randomized study with dose escalation in Phase 1, followed by expansion at a recommended phase 2 dose.


Recruitment information / eligibility

Status Completed
Enrollment 72
Est. completion date June 2018
Est. primary completion date September 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- To be considered eligible to participate in this study, all of the following requirements must be met:

1. Patients in Phase 1 must have metastatic or locally advanced solid tumors who have failed to respond to standard therapy

2. All patients must have confirmation of either ALK positive or TRK positive status.

3. Patients in Phase 1 will not be required to have measurable disease. All patients in Phase 2a will be required to have measurable disease by RECIST.

4. All patients enrolled in this study must have tumor tissue available.

5. Patient (male or female) must be = 18 years of age (except where age of majority is 16 years in a particular country, such as the United Kingdom).

6. Patient must have performance status =2 on the ECOG Performance Scale.

7. Patient must have an estimated life expectancy of at least 3 months.

8. Patients must have adequate organ function.

9. For patients previously treated with myelosuppressive therapy, at least 3 weeks must have elapsed and toxicity must have recovered to grade 1 or baseline. Non-myelosuppressive therapy patients must have recovered from all treatment-related toxicities. Fourteen days must have elapsed since palliative radiation for bone metastasis.

10. Female patients of childbearing potential must have a negative serum pregnancy test and use adequate birth control for the duration of study participation and for 3 months after the last dose of study drug.

11. The patient or his or her legal representative must be able to read, understand, and provide signed informed consent.

12. Patient is able to understand the study procedures and agrees to participate in the study by giving written informed consent.

Exclusion Criteria:

- Patients will not be deemed eligible for entry into this study if any of the following criteria are met:

1. Patient has leukemia.

2. Patient is a pregnant or lactating female.

3. Patient has uncontrolled congestive heart failure, angina, or has had a myocardial infarction in the preceding 3 months.

4. Ongoing cardiac dysrhythmias of NCI CTCAE Grade =2, atrial fibrillation of any grade, or QTc interval >450 msec.

5. Patients with risk factors for Torsade de point and patients receiving concomitant medication with QT-prolonging medicines.

6. Patient has an uncontrolled concurrent medical condition or disease.

7. Patient has undergone bone marrow or stem cell transplantation in the past 6 months.

8. Patient has a known hypersensitivity to the components of TSR-011 or the excipients.

9. Patient has active or uncontrolled infection.

10. Patient has a known psychiatric or substance abuse disorder.

11. Patient has active second primary malignancy.

12. Patient is observed to have a clinically active central nervous system (CNS) metastases or carcinomatous meningitis.

13. Patient has any other severe concurrent disease which, in the judgment of the Investigator, would preclude study participation.

14. Patient is known to be HIV positive or who has an AIDS-related illness.

15. Patient has a known history of or active (treated or not) Hepatitis B or C.

16. Patient has presence of ascites causing significant symptoms.

17. A patient must stop taking any prescription, over-the-counter, or herbal remedy known to be an inhibitor or inducer of CYP3A4/5.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
TSR-011
Number of cycles until progression or unacceptable toxicity develops.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Tesaro, Inc.

Countries where clinical trial is conducted

United States,  Poland,  Spain,  Taiwan,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of Adverse Events (AEs) Approximately 2 years
Secondary Area Under the Concentration-Time Curve (AUC) Day 1: 0-24 hrs after first dose; pre-dose on days 8 & 15; day 29: 0-24 hours
Secondary Maximum Tolerated Dose (MTD) Phase 1, during the dose-escalation phase 28 days after first dose
Secondary Response Rate (RR) Phase 2 approximately 2 years
Secondary Dose limiting toxicity (DLT) Phase 1, during the dose escalation phase 28 days after first dose
Secondary Progression Free Survival (PFS) Phase 2 approximately 2 years
Secondary Recommended Phase 2 Dose (RP2D) Phase 1 approximately 2 years
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