A Study of Pralsetinib Versus Standard of Care (SOC) for Treatment of RET-Mutated Medullary Thyroid Cancer (MTC).

NCT ID: NCT04760288

Last Updated: 2024-01-05

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: PHASE3
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-11-30
• Study Completion Date: 2035-04-12

Brief Summary

A study to evaluate the efficacy and safety of pralsetinib compared with SOC treatment (cabozantinib or vandetanib) for participants with RET (rearranged during transfection)-mutant MTC who have not previously received a SOC MultiKinase Inhibitor (MKI) therapy. Participants will be randomized in a 1:1 ratio into one of two treatment arms: Arm A (pralsetinib) or Arm B (investigator's choice of either cabozantinib or vandetanib for adults and vandetanib for adolescents). Participants whose disease progresses during SOC treatment will be offered the option to cross over to receive pralsetinib after confirmation of progressive disease by blinded independent central review (BICR).

Conditions

Medullary Thyroid Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Arm A (Pralsetinib)

Participants will receive pralsetinib at a dose of 400 milligrams (mg) orally once daily (PO QD) in 28-day cycles.

Group Type: EXPERIMENTAL

Pralsetinib

Intervention Type: DRUG

Participants will receive pralsetinib at a dose of 400 mg, as per the dosing schedule described above.

Arm B (SOC: Cabozantinib/Vandetanib)

Adult participants will receive investigator's choice of SOC MKI therapy with either 140 mg cabozantinib PO QD or 300 mg vandetanib PO QD in 28-day cycles. Adolescents participants (≥ 12 and \< 18 years of age) will receive vandetanib, PO QD or every other day, in 28-day cycles depending on the body surface area (BSA), at a dose determined according to the dosing nomogram available in the E.U. Vandetanib SmPC.

Group Type: ACTIVE_COMPARATOR

Cabozantinib

Intervention Type: DRUG

Adult participants will receive cabozantinib at a dose of 140 mg, as per the dosing schedule described above.

Vandetanib

Intervention Type: DRUG

Adult participants will receive vandetanib at a dose of 300 mg and adolescent participants will receive vandetanib as per the dosing schedule described above.

Interventions

Pralsetinib

Participants will receive pralsetinib at a dose of 400 mg, as per the dosing schedule described above.

Intervention Type: DRUG

Cabozantinib

Adult participants will receive cabozantinib at a dose of 140 mg, as per the dosing schedule described above.

Intervention Type: DRUG

Vandetanib

Adult participants will receive vandetanib at a dose of 300 mg and adolescent participants will receive vandetanib as per the dosing schedule described above.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Must have histologically confirmed unresectable locally advanced or metastatic MTC and be a candidate for systemic therapy with SOC MKI.
• Must have received no prior systemic anticancer treatment with MKI therapies for advanced or metastatic MTC.
• Must have radiologically confirmed progressive disease within the last 14 months and at least one of the following:

1. A MTC-associated symptom and

2. CLN (Calcitonin) and CEA (carcinoembryonic antigen) level doubling time of less than 24 months.

• Confirmed RET mutation.
• Must be able to swallow an oral medication.
• Must have an ECOG (Eastern Cooperative Oncology Group) Performance Status of 0-2.
• For women of childbearing potential: agreement to remain abstinent (refrain from heterosexual intercourse) or use appropriate contraception during the treatment period and for the respective period of time after final dose of study drug.
• For men: agreement to remain abstinent (refrain from heterosexual intercourse) or use appropriate contraception during the treatment period and for the respective period of time after final dose of study drug and to refrain from donating sperm.

Exclusion Criteria

• Participants who are pregnant or breastfeeding, or intending to become pregnant during the study within 14 days after the final dose of pralsetinib or within 4 months after the final dose of vandetanib or cabozantinib.
• Have disease that is suitable for surgery or radiotherapy administered with curative intent.
• Have been previously treated with any systemic kinase inhibitor therapy regimens, including a selective RET inhibitor, given for recurrent and/or metastatic disease.
• Have received any radiation therapy within 14 days prior to Day 1 of Cycle 1 and any related toxicity must be resolved to Grade 1 or better.
• Participant's tumor has any additional known primary driver alterations other than RET.
• Have known hypersensitivity to pralsetinib, vandetanib, or cabozantinib, or any of their ingredients.
• Have a history of pneumonitis of non-infectious etiology within the last 12 months.
• Have ongoing treatment with chronic immunosuppressants or systemic steroids >10 mg/day.
• Have any history of hereditary bleeding disorder or any evidence of hematemesis.
• Have had major surgery or invasive dental procedure within 3 weeks prior to Day 1 of Cycle 1.
• Have central nervous system (CNS) metastases that are associated with progressive neurologic symptoms, untreated spinal cord compression or requires increasing doses of corticosteroids to control the CNS disease.
• Have clinically significant, uncontrolled, cardiovascular disease.
• Have required treatment with a prohibited medication or herbal remedy.
• Have received hematopoietic growth factor support or transfusion within 14 days of the first dose of study drug.
• Had a major surgical procedure within 14 days of the first dose of study drug.
• Have a history of another primary malignancy that has been diagnosed or required therapy within the past 2 years before randomisation.
• Have a serious infection requiring intravenous (IV) antibiotics within 7 days prior to initiation of study treatment.
• Have an active, uncontrolled infection (viral, bacterial, or fungal) or is positive for Hepatitis B/C infections (HBV/HCV) or HIV.
• Have received organ or allogenic bone marrow or peripheral blood stem cell transplant.
• Is a female who is unwilling to abstain from sexual intercourse or employ highly effective contraception from the time of informed consent and for at least 4 months after the last dose of study drug.
• Is a male who is unwilling to abstain from sexual intercourse or employ highly effective contraception from the time of informed consent and for at least 120 days after the final dose of study drug.
• Have prior or ongoing clinically significant illness, medical condition, surgical history, physical finding, or laboratory abnormality that, in the Investigator's or Sponsor's opinion, could affect the safety of the patient or impair the assessment of study results.

• Minimum Eligible Age: 12 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Hoffmann-La Roche

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Clinical Trials

Role: STUDY_DIRECTOR

Hoffmann-La Roche

Locations

Hospital Universitario Virgen del Rocio

Seville, , Spain

Countries

Spain

Other Identifiers

2020-005269-15

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

CO42865

Identifier Type: -

Identifier Source: org_study_id