A Study of Tinengotinib (TT-00420) in Combination With Standard Treatments in People With Prostate Cancer

Trial statusRecruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexMale
Age18+
SponsorMemorial Sloan Kettering Cancer Center

About this trial

The purpose of this study is to find out whether tinengotinib in combination with abiraterone acetate and prednisone or enzalutamide is a safe treatment that causes few or mild side effects in people with metastatic castration-resistant prostate cancer (mCRPC).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Participants ≥ 18 years old, with signed informed consent

Histologically confirmed carcinoma of the prostate (neuroendocrine differentiation is allowed, but pure small cell carcinoma is not permitted)

Metastatic disease documented by at least 2 bone lesions on whole body radionuclide bone scan, or soft tissue disease documented by computed tomography (CT) scan/magnetic resonance imaging (MRI). Note: Metastatic disease seen only on PET imaging does not qualify.

Current ongoing therapy and observed tolerance with full standard dose of abiraterone acetate (1000 mg QD) or enzalutamide (160 mg QD) at the time of study entry. Enzalutamide or abiraterone acetate must have been started at least 90 days before screening assessments. An interruption of dosing of a maximum of 30 days is permitted prior to resuming the agent. Please note: Patients who are on a reduced dose or are intolerant of abiraterone acetate or enzalutamide at screening will not be eligible for study participation.

Disqualifiers

Pure small cell carcinoma

Previous exposure to multi-TKI therapies.

Uncontrolled hypertension (persistent systolic blood pressure ≥ 140 mm Hg and/or diastolic blood pressure ≥ 90 mm Hg) or known coronary artery disease with angina. Patients with known hypertension must be on antihypertensive medication with BPs generally <140/90 to be eligible.

History of congestive heart failure of Class II-IV New York Heart Association criteria, or serious cardiac arrhythmia requiring treatment (except atrial fibrillation, paroxysmal supraventricular tachycardia), history of myocardial infarction within 6 months of study entry, or prolongation of QTc interval to >480 msec using Fridericia formula (QTcF) at screening (except for participants with pacemakers, where there is no QTc cutoff).

Trial design

Design model

Sequential

Treatments tested in this trial

  • Tinengotinib

    Drug

    Tinengotinib will be administered daily for 28-day cycles. A flat dose of 10 mg PO once daily.

  • abiraterone acetate with prednisone

    Drug

    Abiraterone acetate 1000 mg PO QD in combination with prednisone 5 mg PO once or twice daily (QD or BID)

  • Enzalutamide

    Drug

    Enzalutamide 160 mg PO QD

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: Tinengotinib with abiraterone acetate/prednisoneExperimental treatment 2 interventions
Group B: Tinengotinib with enzalutamideExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

RP2D

Evaluate DLT occurrence to confirm safety and RP2D

Time frame
From the start of study treatment through the DLT window (28 days)
2

Objective Response Rate (ORR)

by local investigator's assessment per PCWG3-modified RECIST v1.1 in participants with baseline measurable disease OR rate of PSA decline of ≥ 50% from baseline in patients with a baseline PSA of 2.0 ng/mL or above

Time frame
up to 6months

Secondary outcomes

1

Rate of Radiographic Response (phase II)

Rate of radiographic response by local investigator's assessment per PCWG3-modified RECIST v1.1 in participants with baseline measurable disease

Time frame
From start of study treatment until 6 months post study treatment start

Other outcomes

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