Study of XL114 in Subjects With Non-Hodgkin's Lymphoma

Sponsor

Exelixis (Industry)

Overall Status

Recruiting

CT.gov ID

NCT05144347

Collaborator

(none)

144

Enrollment

Locations

Arms

Anticipated Duration (Months)

Patients Per Site

1.6

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This is a Phase 1, non-randomized, open-label, dose-escalation and expansion study, evaluating the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary clinical antitumor activity of XL114 administered alone orally to subjects with Non-Hodgkin's Lymphoma (NHL). The objectives of the study also include determining the recommended dose (RD) and/or maximum tolerated dose (MTD) of XL114.

Condition or Disease	Intervention/Treatment	Phase
Non-Hodgkin's Lymphoma (NHL) Activated B-Cell Type Diffuse Large B-Cell Lymphoma (ABC-DLBCL) Mantle Cell Lymphoma (MCL) Chronic Lymphocytic Leukemia (CLL) Small Lymphocytic Lymphoma (SLL)	Drug: XL114	Phase 1

Study Design

Study Type:

Interventional

Anticipated Enrollment :

144 participants

Allocation:

Non-Randomized

Intervention Model:

Sequential Assignment

Intervention Model Description:

Dose-escalation followed by Cohort-expansion in NHL-specific expansion cohortsDose-escalation followed by Cohort-expansion in NHL-specific expansion cohorts

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

A Dose-Escalation and Expansion Study of the Safety and Pharmacokinetics of XL114 Administered in Subjects With Non-Hodgkin's Lymphoma

Actual Study Start Date :

Apr 12, 2022

Anticipated Primary Completion Date :

Dec 11, 2025

Anticipated Study Completion Date :

Dec 11, 2025

Arms and Interventions

Arm	Intervention/Treatment
Experimental: XL114 Dose-Escalation Cohorts Subjects (Cohort A1-An) will accrue in cohorts of 3-12 subjects in a i3+3 design.	Drug: XL114 Tablets of XL114
Experimental: XL114 Expansion Cohorts The recommended dose from the Dose-Escalation stage, will be used in subjects with activated B-cell-like diffuse large B-cell lymphoma [ABC-DLBCL] (Cohort B), mantle cell lymphoma [MCL] (Cohort C), chronic lymphocytic leukemia [CLL]/small lymphocytic lymphoma [SLL] (Cohort D). Subjects will also be enrolled in a Biomarker cohort (Cohort E).	Drug: XL114 Tablets of XL114

Arm

Intervention/Treatment

Experimental: XL114 Dose-Escalation Cohorts

Subjects (Cohort A1-An) will accrue in cohorts of 3-12 subjects in a i3+3 design.

Drug: XL114

Tablets of XL114

Experimental: XL114 Expansion Cohorts

The recommended dose from the Dose-Escalation stage, will be used in subjects with activated B-cell-like diffuse large B-cell lymphoma [ABC-DLBCL] (Cohort B), mantle cell lymphoma [MCL] (Cohort C), chronic lymphocytic leukemia [CLL]/small lymphocytic lymphoma [SLL] (Cohort D). Subjects will also be enrolled in a Biomarker cohort (Cohort E).

Drug: XL114

Tablets of XL114

Outcome Measures

Primary Outcome Measures

Dose-Escalation Stage: Recommended Dose (RD) and/or Maximum Tolerated Dose (MTD) for XL114 [4-6 months]
To determine the RD and/or MTD of XL114 administered orally in subjects with NHL
Cohort-Expansion Stage: Objective Response Rate (ORR) [4-6 months]
To evaluate preliminary efficacy of XL114 by estimating the ORR based on lymphoma-specific response criteria as assessed by the Investigator

Secondary Outcome Measures

Safety of XL114, as evaluated by Adverse Events (AEs) [4-6 months]
To evaluate the safety of XL114 through the evaluation of incidence and severity of treatment emergent nonserious adverse events (AEs) and serious adverse events (SAEs)at each dose level and their relationship to study drug treatment.
Tolerability of XL114, as evaluated by Dose Intensity, Dose Modifications, and Study Discontinuation due to AEs [4-6 months]
To evaluate the tolerability of XL114 through the evaluation of dose intensity, dose modifications and study treatment discontinuation due to AEs related to XL114.
Dose-Escalation Stage: Time to Maximum Plasma Concentration (Tmax) [4-6 months]
To evaluate the Tmax of XL114.
Dose-Escalation Stage: Maximum Plasma Concentration (Cmax) [4-6 months]
To evaluate the Cmax of XL114.
Dose-Escalation Stage: Area Under the Plasma Concentration-Time Curve Over the Last 24-hour Dosing Interval (AUC 0-24) [4-6 months]
To evaluate the AUC 0-24 of XL114.
Dose-Escalation Stage: Terminal Half-Life [4-6 months]
To evaluate the terminal half-life of XL114.
Dose-Escalation Stage: Apparent Clearance (CL/F) [4-6 months]
To evaluate the CL/F of XL114.
Cohort-Expansion Stage: Antitumor Activity of XL114 (Objective Response Rate [ORR]) [4-6 months]
To evaluate the antitumor activity of XL114 as measured by ORR based on lymphoma-specific response criteria as assessed by a Blinded Independent Radiology Committee (BIRC) for selected cohorts.
Cohort-Expansion Stage: Antitumor Activity of XL114 (Duration of Response [DOR]) [4-6 months]
To evaluate the antitumor activity of XL114 as measured by DOR based on lymphoma-specific response criteria as assessed by the Investigator or by a Blinded Independent Radiology Committee (BIRC) for selected cohorts.
Cohort-Expansion Stage: Antitumor Activity of XL114 (Progression Free Survival [PFS]) [4-6 months]
To evaluate the antitumor activity of XL114 as measured by PFS based on lymphoma-specific response criteria as assessed by the Investigator or by a Blinded Independent Radiology Committee (BIRC) for selected cohorts.
Cohort-Expansion Stage: Overall Survival (OS) of XL114 [4-6 months]
To evaluate duration of overall survival (OS)

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Dose-Escalation Stage (Cohort A) and Cohort-Expansion Stage (B-E): The subject has received standard life-prolonging therapies or are not qualified to receive such therapies.
Dose-Escalation Stage (Cohort A): Subjects with histologically documented diagnosis of B-cell or T-cell Non-Hodgkin's Lymphoma as defined by the World Health Organization (WHO) classification. Note: Refer to exclusion criteria for lymphoma subtypes which are excluded from study participation.
Cohort-Expansion Stage Cohort B (ABC-DLBCL subtype): Subjects with histologically documented activated B-cell diffuse large B-cell lymphoma (ABC-DLBCL) subtype. Note: De novo or transformed diffuse large B-cell lymphoma (DLBCL) from previously diagnosed indolent lymphoma (eg, follicular lymphoma) is allowed.
Cohort-Expansion Stage Cohort C (MCL): Subjects with histologically documented MCL with monoclonal B-cells that show a chromosome translocation t(11;14)(q13;q32) and/or overexpression of cyclin D1.
Cohort-Expansion Stage Cohort D (CLL/SLL): Subjects with histologically documented CLL/SLL per the International Workshop on Chronic Lymphocytic Leukemia (iwCLL) guidelines.
Cohort-Expansion Stage Cohort E, Biomarker Cohort (ABC-DLBCL, MCL, and SLL): Subjects with ABC-DLBCL, MCL, and SLL that fulfill the subject disease characteristics criteria as described for Cohorts B, C, or D.
Cohort-Expansion Stage: Subjects with ABC-DLBCL, MCL, and SLL must have measurable disease by revised criteria for response assessment of lymphoma.
Cohort-Expansion Stages: Must have archival tumor tissue available, which was collected up to 2 years prior to consent for this study. If archival tumor tissue is not available, a fresh tumor biopsy may be obtained (if safe to acquire) up to 60 days prior to first dose.
Biomarker Cohort: Subjects must provide a fresh tumor biopsy up to 60 days prior to first dose, at week 2, day 1 (W2D1) after initiation of XL114, and at disease progression. Note: The tumor tissue requirement in the Expansion and Biomarker cohorts doesn't apply for subjects with CLL.
Recovery to baseline or ≤ Grade 1 severity (Common Terminology Criteria for Adverse Events version 5 [CTCAE v5]) from AEs, unless AEs are clinically nonsignificant or stable.
Left ventricular ejection fraction (LVEF) > 50% as determined by echocardiogram (ECHO) or multigated acquisition (MUGA) scan per local standard.
Age 18 years or older on the day of consent.
Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0-1
Adequate organ and marrow function
Sexually active fertile subjects and their partners must agree to highly effective methods of contraception.
Female subjects of childbearing potential must not be pregnant at screening.

Exclusion Criteria:

Receipt of prior therapies as defined in the protocol
The following lymphoma types/manifestations are not eligible for this study: Burkitt's lymphoma (BL), Burkitt-like lymphoma (BLL), lymphoblastic lymphoma/leukemia (LBL), post-transplant lymphoproliferative disease (PTLD), primary mediastinal (thymic) large B-cell lymphoma (PMBL), lymphomas involving the central nervous system (CNS) or meninges
History of autoimmune hemolytic anemia (AIHA) or idiopathic thrombocytopenic purpura (ITP).
History of solid organ or allogeneic hematopoietic stem cell transplantation.
Concomitant anticoagulation with the oral anticoagulants apixaban, betrixaban, rivaroxaban, and dabigatran.
Use of a strong inhibitor or inducer of cytochrome P450 3A4 (CYP3A4) within 5 half-lives or 4 weeks prior to first dose of study treatment, whichever is shorter.
Uncontrolled, significant intercurrent or recent illness
Major surgery (eg, GI surgery) within 3 weeks before first dose of study treatment.
Corrected QT interval calculated by the Fridericia formula (QTcF) > 470 ms per electrocardiogram (ECG).
Pregnant or lactating females.
Inability to swallow XL114 tablets.
Diagnosis of another malignancy within 2 years before first dose of study treatment, except for superficial skin cancers, or localized, low-grade tumors deemed cured and not treated with systemic therapy