Study of TP-3654 in Patients With Advanced Solid Tumors

Sponsor

Sumitomo Pharma Oncology, Inc. (Industry)

Overall Status

Completed

CT.gov ID

NCT03715504

Collaborator

(none)

Enrollment

Locations

Arm

26.7

Actual Duration (Months)

7.3

Patients Per Site

0.3

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

TP-3654 is an oral PIM inhibitor. This is a Phase 1, open-label, dose-escalation, safety, pharmacokinetics, and pharmacodynamic study, with a purpose of determining the maximum tolerated dose (MTD) and dose-limiting toxicities (DLTs) of oral TP-3654 in patients with advanced solid tumors.

Condition or Disease	Intervention/Treatment	Phase
Advanced Solid Tumors	Drug: TP-3654	Phase 1

Detailed Description

Primary Objective:

• To determine the maximum tolerated dose (MTD) and dose-limiting toxicities (DLTs) of oral TP-3654 in patients with advanced solid tumors.

Secondary Objectives:

To establish the pharmacokinetic (PK) profile of orally administered TP-3654
To observe patients for any evidence of antitumor activity of TP-3654 by objective radiographic assessment
To study the pharmacodynamic effects of TP-3654 therapy
To establish the Recommended Phase 2 Dose (RP2D) for future studies with TP-3654

Study Design

Study Type:

Interventional

Actual Enrollment :

22 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

A Phase I, First-in-human, Open-label, Dose Escalation, Safety, Pharmacokinetic, and Pharmacodynamic Study of Oral TP-3654 in Patients With Advanced Solid Tumors

Actual Study Start Date :

Apr 16, 2019

Actual Primary Completion Date :

Mar 30, 2021

Actual Study Completion Date :

Jul 8, 2021

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Single Arm TP-3654 TP-3654 by oral administration	Drug: TP-3654 oral PIM inhibitor

Arm

Intervention/Treatment

Experimental: Single Arm TP-3654

TP-3654 by oral administration

Drug: TP-3654

oral PIM inhibitor

Outcome Measures

Primary Outcome Measures

Incidence of dose-limiting toxicities (DLTs) and treatment emergent adverse events [28 days]
Determine maximum tolerated dose (MTD) [20 months]
MTD will be determined based upon toxicity grades which are defined by the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE).

Secondary Outcome Measures

Recommended Phase 2 Dose of TP-3654 [23 months]
To establish the Recommended Phase 2 Dose (RP2D) for future studies with TP-3654, MTD data to be reviewed
Determine antitumor activity of TP-3654 [20 months]
Assess for tumor burden by radiological assessment (computed tomography [CT] imaging) using RECIST v1.1

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

1. Have a histologically confirmed diagnosis of advanced metastatic, progressive or unresectable solid tumor

Be refractory to, or intolerant of, established therapy known to provide clinical benefit for their condition.
Have 1 or more tumors measurable or evaluable as outlined by modified Response Evaluation Criteria in Solid Tumors (RECIST) v1.1
Have an Eastern Cooperative Oncology Group (ECOG) performance status of less than or equal to 2
Have a life expectancy greater than or equal to 3 months
Be greater than or equal to 18 years of age
Have a negative pregnancy test (if female of childbearing potential) and not currently nursing
Have acceptable liver function:

Bilirubin less than or equal to 1.5x upper limit of normal (ULN) (unless associated with Gilbert's syndrome b. Aspartate aminotransferase (AST/SGOT), alanine aminotransferase (ALT/SGPT) and alkaline phosphatase less than or equal to 2.5x upper limit of normal (ULN) *If liver metastases are present, then less than or equal to 5x ULN is allowed.

Have acceptable renal function:

Calculated creatinine clearance greater than or equal to 30 mL/min

Have acceptable hematologic status:

Absolute Neutrophil Count (ANC) greater than or equal to 1500 x10^{9/L b. Platelet
count greater than or equal to 100,000 x 10}9/L c. Hemoglobin greater than or equal to 8 g/dL

Have acceptable coagulation status:
Prothrombin time (PT) within 1.5 x normal limits
Activated partial thromboplastin time (aPTT) within 1.5 x normal limits
Be nonfertile or agree to use an adequate method of contraception. Sexually active patients and their partners must use an effective method of contraception (hormonal or barrier method of birth control; or abstinence) prior to study entry and for the duration of study participation and for 3 months (males) and 6 months (females) after the last study drug dose. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.
Have read and signed the Institutional Review Board (IRB)-approved informed consent form prior to any study related procedure. (In the event that the patient is re-screened for study participation or a protocol amendment alters the care of an ongoing patient, a new informed consent form must be signed.)

Exclusion Criteria:

1. History of congestive heart failure (CHF), Cardiac disease, myocardial infarction within the past 6 months prior to Cycle 1 Day 1, left ventricular ejection fraction <45% by echocardiogram, unstable arrhythmia, or evidence of ischemia on electrocardiogram (ECG) within 14 days prior to Cycle 1 Day 1

Have a corrected QT interval (using Fridericia's correction formula) (QTcF) of >450 msec in men and >470 msec in women
Presence of symptomatic central nervous system metastatic disease or disease that requires local therapy such as radiotherapy, surgery, or increasing dose of steroids within the prior 2 weeks.
Have severe chronic obstructive pulmonary disease with hypoxemia (defined as resting 02 saturation of less than or equal to 90% breathing room air). The use of supplemental oxygen with nasal cannula to reach >90% saturation will not preclude study participation.
Have undergone major surgery, other than diagnostic surgery, within 2 weeks prior to Cycle 1 Day 1
Have active, uncontrolled bacterial, viral, or fungal infections, requiring systemic therapy
Received treatment with radiation therapy, surgery, chemotherapy, or investigational therapy within 28 days or 5 half-lives, whichever occurs first, prior to study entry (6 weeks for nitrosoureas or Mitomycin C)

8, Are unwilling or unable to comply with procedures required in this protocol

Have known infection with human immunodeficiency virus, hepatitis B, or hepatitis

Patients with history of chronic hepatitis that is currently not active are eligible.

Have a serious nonmalignant disease (eg, hydronephrosis, liver failure, or other conditions) that could compromise protocol objectives in the opinion of the Investigator and/or the Sponsor
Are currently receiving any other investigational agent
Have exhibited allergic reactions to a similar structural compound, biological agent, or formulation
Have a medical conditional such as Crohn's disease or have undergone significant surgery to the gastrointestinal tract that could impair absorption or that could result in short bowel syndrome with diarrhea due to malabsorption.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	MD Anderson	Houston	Texas	United States	77030
2	Huntsman Cancer Institute	Salt Lake City	Utah	United States	84112
3	University of Virginia	Charlottesville	Virginia	United States	22903