Last updated: 07/17/2024 16:56:35

A study to investigate the safety, pharmacokinetics, pharmacodynamics and clinical activity of GSK2816126 in subjects with relapsed/refractory diffuse large B cell lymphoma, transformed follicular lymphoma, other Non-Hodgkin’s lymphomas, solid tumors and multiple myeloma

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GSK study ID

117208

See study documents

Clinicaltrials.gov ID

NCT02082977

See results summary

EudraCT ID

2013-001585-42

EU CT Number

Not applicable

Trial status

Terminated (halted prematurely)

Overview

Eligibility

Locations

Study documents

Results summary

Plain language summaries

Additional information

Trial overview

Official title: A phase I open-label, dose escalation study to investigate the safety, pharmacokinetics, pharmacodynamics and clinical activity of GSK2816126 in subjects with relapsed/refractory diffuse large B cell lymphoma, transformed follicular lymphoma, other Non-Hodgkin’s lymphomas, solid tumors and multiple myeloma

Trial description: This is an open-label, multicenter, 2-part study to determine the recommended Phase 2 dose (RP2D) for GSK2816126 given twice weekly by intravenous (IV) infusion. Part 1 will be conducted in adult subjects with relapsed/refractory diffuse large B cell lymphoma (DLBCL), transformed follicular lymphoma (tFL), other Non-Hodgkin’s lymphomas (NHL), solid tumors (including castrate resistant prostate cancer) and multiple myeloma (MM) to determine the safety and tolerability of GSK2816126. Expansion cohorts (Part 2) are planned to further explore clinical activity of GSK2816126 at the RP2D in subjects with Enhancer of Zeste 2 (EZH2) wild type and EZH2 mutant positive germinal center B-cell like diffuse large B cell lymphoma (GCB-DLBCL), tFL and MM.

Primary purpose:

Treatment

Trial design:

Sequential Assignment

Masking:

None (Open Label)

Allocation:

Non-randomized

Primary outcomes:

Part 1: Number of participants with serious adverse events (SAEs) and non-serious adverse events (Non-SAEs)

Timeframe: Up to 3.2 years

Part 1: Number of participants with dose limiting toxicities (DLT)

Timeframe: Up to 4 weeks

Part 1: Number of participants withdrawn due to AEs

Timeframe: Up to 3.2 years

Part 1: Number of participants with dose interruptions

Timeframe: Up to 3.2 years

Part 1: Number of participants with dose reductions

Timeframe: Up to 3.2 years

Part 1: Number of participants with worst case change from Baseline in clinical chemistry parameters

Timeframe: Baseline and up to 3.2 years

Part 1: Number of participants with worst case change from Baseline in hematology parameters

Timeframe: Baseline and up to 3.2 years

Part 1:Number of participants with abnormal values for vital signs

Timeframe: Up to 3.2 years

Part 1: Number of participants with abnormal findings for electrocardiogram (ECG) parameters

Timeframe: Up to 3.2 years

Part 2: Percentage of participants achieving overall response rate

Timeframe: Up to 3.2 years

Secondary outcomes:

Part 1: Area under the concentration-time curve from time zero (pre-dose) to last time of quantifiable concentration (AUC [0-t]) following single and repeat dose administration of GSK2816126

Timeframe: Pre-dose, 0.5, 1, 2, (12, 18 on Day 1 only), 24, and 96 hours post-dose from start of infusion; 0.5, 1, 2, 4, 6 hours from end of infusion on Cycle 1 of Day 1 and Day 15 (Each cycle was of 28 days)

Part 1: Area under the concentration-time curve from time zero (pre-dose) extrapolated to infinite time (AUC [0-infinity]) following single dose administration of GSK2816126

Timeframe: Pre-dose, 0.5, 1, 2, 12, 18 , 24, and 96 hours post-dose from start of infusion; 0.5, 1, 2, 4, 6 hours from end of infusion on Cycle 1 of Day 1 (Each cycle was of 28 days)

Part 1: Area under the concentration-time curve over the dosing interval (AUC [0-tau]) following repeat dose administration of GSK2816126

Timeframe: Pre-dose, 0.5, 1, 2, 24, and 96 hours post-dose from start of infusion; 0.5, 1, 2, 4, 6 hours from end of infusion on Cycle 1 of Day 15 (Each cycle was of 28 days)

Part 1: Trough (pre-dose) concentration at the end of dosing interval on the specified days (Ctau) following administration of GSK2816126

Timeframe: Pre-dose from start of infusion till end of infusion on Cycle 1 of Day 8; Pre-dose, 0.5, 1, 2, 24, and 96 hours post-dose from start of infusion; 0.5, 1, 2, 4, 6 hours from end of infusion on Cycle 1 of Day 15 (Each cycle was of 28 days)

Part 1: Maximum observed plasma concentration (Cmax) following single and repeat dose administration of GSK2816126

Part 1: Time to reach Cmax (Tmax) following single and repeat dose administration of GSK2816126

Part 1: Apparent terminal phase elimination rate constant (lambda z) following single and repeat dose administration of GSK2816126

Part 1: Apparent terminal phase half-life (T1/2) following single and repeat dose administration of GSK2816126

Part 1: Accumulation ratio following administration of GSK2816126

Part 1: Time invariance ratio following administration of GSK2816126

Part 1: Exposure producing 50 percent of the maximum effect (EC50) of GSK2816126 with respect to exposure markers

Timeframe: Up to 3.2 years

Part 1: Maximum effect (Emax) of GSK2816126 with respect to exposure markers

Timeframe: Up to 3.2 years

Part 1: Number of participants with overall change in Tri-methylated Histone H3 lysine 27 (H3K27me3) ratios compared to Baseline

Timeframe: Baseline and up to 3.2 years

Part 1: Percentage of participants with solid tumors achieving best overall response rate

Timeframe: Up to 3.2 years

Part 1: Percentage of participants with lymphoma achieving best overall response rate

Timeframe: Up to 3.2 years

Part 1: Concentration of GSK2816126 and its metabolites in blood

Part 1: Concentration of GSK2816126 and its metabolites in bile

Timeframe: Day 15

Part 1: Concentration of GSK2816126 and its metabolites in urine

Timeframe: Pre-dose and 0 to 24 hours post-dose on Day 1; 0 to 8 hours post-dose on Day 15

Part 1:Concentration of GSK2816126 in urine after dosing at steady state

Timeframe: Pre-dose and 0 to 24 hours post-dose on Day 1; 0 to 8 hours post-dose on Day 15

Part 2: Number of participants with SAEs and Non-SAEs

Timeframe: Up to 3.2 years

Part 2: Number of participants with DLTs

Timeframe: Up to 4 weeks

Part 2: Number of participants withdrawn due to AEs

Timeframe: Up to 3.2 years

Part 2: Number of participants with dose interruptions

Timeframe: Up to 3.2 years

Part 2: Number of participants with dose reductions

Timeframe: Up to 3.2 years

Part 2: Number of participants with worst case change from Baseline in clinical chemistry parameters

Timeframe: Baseline and up to 3.2 years

Part 2: Number of participants with worst case changes from Baseline in hematology parameters

Timeframe: Baseline and up to 3.2 years

Part 2: Number of participants with abnormal values for vital signs

Timeframe: Up to 3.2 years

Part 2: Number of participants with abnormal findings for ECG parameters

Timeframe: Up to 3.2 years

Part 2: Clearance following administration of GSK2816126

Timeframe: Up to 3.2 years

Part 2: Volume of distribution following administration of GSK2816126

Timeframe: Up to 3.2 years

Part 2:EC50 of GSK2816126 with respect to exposure markers

Timeframe: Up to 3.2 years

Part 2:Emax of GSK2816126 with respect to exposure markers

Timeframe: Up to 3.2 years

Part 2: Number of participants with change in H3K27me3 ratios compared to Baseline

Timeframe: Baseline and up to 3.2 years

Part 2: Concentration of GSK2816126 and its metabolites in blood

Timeframe: Pre-dose, single draw between 0.5 and 1.9 hours from start of infusion, single draw between 3-6 hours following end of infusion on Day 1; Pre-dose on Day 15 for Cycle 1 and Cycles 2, 4, 6 and 12 (Each cycle was of 28 days)

Part 2: Concentration of GSK2816126 and its metabolites in bile

Timeframe: Day 15

Part 2: Concentration of GSK2816126 and its metabolites in urine

Timeframe: Pre-dose and 0 to 24 hours post-dose on Day 1; 0 to 8 hours post-dose on Day 15

Part 2:Concentration of GSK2816126 in urine after dosing at steady state

Timeframe: Pre-dose and 0 to 24 hours post-dose on Day 1; 0 to 8 hours post-dose on Day 15

Part 2: Change in 4-beta-hydroxy cholesterol to cholesterol ratio from Baseline following repeat dosing of GSK2816126

Timeframe: Baseline and up to 21 days

Part 2: Duration of response

Timeframe: Up to 3.2 years

Part 2: Number of participants with progression free survival

Timeframe: Up to 3.2 years

Interventions:

Drug: GSK2816126

Enrollment:

Observational study model:

Not applicable

Primary completion date:

2017-20-06

Time perspective:

Not applicable

Clinical publications:

Yap T, Winter JN, Giulino-Roth L, Longley J, Lopez J, Michot J-M, Leonard JP, Ribrag V, McCabe MT, Creasy CL, Stern M, Dumitrescu TP, Wang X, Frey S, Carver J, Horner T, Oh C, Khaled A, Dhar A, Johnson PWM. Phase 1 study of the novel enhancer of zeste homolog 2 inhibitor GSK2816126 in patients with advanced hematological and solid tumors. Clin. Cancer Res. 2019 DOI: 31471312 PMID: 31471312

Medical condition

Cancer, Neoplasms

Product

GSK2816126

Collaborators

Not applicable

Study date(s)

April 2014 to June 2017

Type

Interventional

Phase

Participation criteria

Sex

Female & Male

Age

18+ years

Accepts healthy volunteers

Part 1 Inclusion Criteria
Provided signed written informed consent

Inclusion and exclusion criteria

Inclusion criteria:

Part 1 Inclusion Criteria
Provided signed written informed consent
Males and females >=18 years of age (at the time consent is obtained).
Tumor type criteria: relapsed/refractory non-Hodgkin’s lymphoma (NHL) that meets one of the following criteria:
Germinal Center B cell Diffuse large B cell lymphoma (GCB-DLBCL) relapsed or refractory to at least one prior regimen (e.g., rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone [R-CHOP]) AND not a candidate for standard salvage regimens or autologous or allogeneic stem cell transplant. Local confirmation of lymphoma subtype (e.g. GCB-DLBCL) is allowed for enrollment but must be confirmed through central laboratory testing.
Solid tumors that meet the following criteria: Measurable disease by Response Evaluation Criteria In Solid Tumors 1.1 (RECIST) in at least 1 site. For Castrate Resistant Prostate Cancer (CRPC) measurable disease can also include Prostate Specific Antigen (PSA) level. Disease progression with the last line of therapy and at least one prior standard of care regimens, or tumor for which there is no approved therapy, or for which standard therapy is unsuitable or refused. Mutation Status: Solid tumor types, other than prostate, must have a one of the following EZH2 inhibitor sensitizing mutations as determined via local testing: An activating mutation in EZH2 (Y641F/C/S/H/N, A677V/G, and/or A687V; Loss of a component of the SWI/SNF complex, including, but not limited to, ARID1A, SMARCB1 (aka SNF5/INI1/BAF47), SMARCA4 (aka BRG1), or PBRM1 (aka PB1) as determined by molecular testing (bi-allelic loss or mutation) or immunohistochemistry; Loss of BAP1 (ubiquitin carboxy-terminal hydrolase) as determined by molecular testing (bi-allelic loss or mutation) or immunohistochemistry
CRPC subjects: Must have measurable disease by either: RECIST1.1 or a minimum PSA of 5 nanogram/milliliter; Disease progression on last line of therapy and must have progressed on abiraterone, enzalutamide, or taxane chemotherapy; Subjects may continue GnRH agonists; Small cell prostate cancer is eligible
For all subjects: Availability of archival tissue, or willingness to undergo fresh biopsy if archival tissue is not available.
Must have a pre-existing central venous access such as a port, Hickmann catheter or a peripherally inserted central catheter (PICC line) or be willing and able to have one inserted.
Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1.
Men with a female partner of childbearing potential must have either had a prior bilateral vasectomy with resultant azoospermia, bilateral orchiectomy, or must agree to use one of the contraception methods listed in protocol from the time of the first dose of study medication until at least 2 weeks (14 days) after the last dose of study treatment due to the long elimination phase of study drug.
A female subject is eligible to participate ifs she is of: Non-child bearing potential as described in the protocol; OR Child bearing potential and agrees to use effective contraception as described in the protocol, for an appropriate period of time (as determined by the product label) prior to the start of dosing to sufficiently minimize the risk of pregnancy and for at least 2 weeks (14 days) following the last dose of study treatment. Women of childbearing potential must have a negative serum pregnancy test within 7 days of first dose of study treatment followed by negative urine or serum pregnancy test once every 4 weeks (prior to next dose cycle) thereafter.- Adequate organ system function as defined in the protocol. Part 2 Inclusion Criteria
In addition to inclusion criteria listed for Part 1, Part 2 will enroll GCB-DLBCL tFL and MM subjects only. Relapsed and/or refractory MM or tFL that have failed prior standard therapy and for which there is no standard salvage regimen
Lymphoma subjects will be required to undergo EZH2 mutation testing. This will require availability of archival tissue, or willingness to undergo fresh biopsy, for central testing of EZH2 mutation status.
Based on the results of the mutation test, lymphoma subjects may be enrolled in one of four cohorts: GCB-DLBCL EZH2 mutant cohort: Tumors must contain one, or more, of the following EZH2 activating mutations: Y641F; Y641N; Y641S; Y641H; Y641C; A677G; and/or A687V. GCB-DLBCL EZH2 wild type cohort: Tumors that do not contain one of the above mutations; Subjects with tumors harboring EZH2 mutations other than the seven outlined above will be enrolled in the EZH2 wild type cohort. tFL EZH2 mutant cohort: Tumors must contain one, or more, of the following EZH2 activating mutations: Y641F; Y641N; Y641S; Y641H; Y641C; A677G; and/or A687V. tFL EZH2 wild type cohort: Tumors that do not contain one of the above mutations; Subjects with tumors harboring EZH2 mutations other than the seven outlined above will be enrolled in the EZH2 wild type cohort Part 1 and 2 Exclusion Criteria
Receiving any cancer therapy within 2 weeks of first dose (including surgery, and/or tumor embolization) Note: the following are allowed: Corticosteroids to control systemic or local symptoms, up to a dose of 10 mg prednisone or equivalent daily and stable for at least 7 days prior to enrollment. Subjects with prostate cancer may remain on GnRH agonists. Other hormonal therapies (e.g., bicalutamide, abiraterone and enzlutimide) for prostate cancer must be stopped 4 weeks prior to enrolment. Note: the following are NOT allowed: Chemotherapy regimens with delayed toxicity within the last 3 weeks. Nitrogen mustards, Melphalan, Monoclonal antibody or Nitrosourea within the last 6 weeks.
Received an investigational anti-cancer drug within 6weeks, or within 5 half-lives (whichever is shorter) of the first dose of study drug(s). A minimum of 14 days must have passed between the last dose of prior investigational agent and the first dose of study drug.
Current use of a prohibited medication per protocol or expected to require any of these medications during treatment with study drug.
Known Human Immunodeficiency Virus, or serological evidence for Hepatitis B (positive hepatitis B surface antigen [HBsAg]), or chronic Hepatitis C infection. For subjects who are negative for HBsAg, but Hepatitis B core Antibody [HBcAB] positive, a HBV DNA (viral load) test will be performed and if negative are eligible. Subjects with positive Hepatitis C antibody serology with a negative HCV ribonucleic acid (RNA) test results are eligible.
Concurrent use of therapeutic warfarin is allowed. However, anticoagulants that do not have reversal agents available are prohibited.
Any major surgery, radiotherapy or immunotherapy within the 4 weeks prior to first dose of study drug, or palliative radiotherapy to a single symptomatic lesion within the 2 weeks prior to first dose of study drugs.
Subjects with prior allogeneic transplant are excluded: however, subjects who have previously received an autologous stem cell transplant are allowed if a minimum of 100 days has elapsed from the time of transplant and the subject has recovered from transplant-associated toxicities prior to the first dose of GSK2816126
Unresolved toxicity greater than Grade 1 National Cancer Institute – Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 4 from previous anti-cancer therapy, with the exception of alopecia and peripheral neuropathy. Lymphoma subjects with <= Grade 3 lymphopenia can be enrolled at the discretion of the investigator.
Packed red blood cell or platelet transfusion within 7 days of screening laboratory tests.
Psychological, familial, sociological or geographical conditions that do not permit compliance with the protocol.
Cardiac exclusion criteria: History of acute coronary syndromes (including myocardial infarction and unstable angina), coronary angioplasty, or stenting within the past 6 months prior to first dose of study drug; QTcF> 450 milliseconds (msec); Uncontrolled arrhythmias. Subjects with rate controlled atrial fibrillation for >1 month prior to first dose of study drug may be eligible; Class II, III or IV heart failure as defined by the New York Heart Association (NYHA) functional classification system.
Known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to the study drug or their excipients.
Pregnant or lactating female.
Unwillingness or inability to follow the procedures outlined in the protocol.
Uncontrolled diabetes or other medical condition that may interfere with assessment of toxicity.
Central nervous system (CNS) metastases, with the following exception: Subjects who have previously treated CNS metastases, are asymptomatic, and have no requirement for steroids at least 14 days prior to first dose of study drug; Subjects with carcinomatous meningitis are excluded regardless of clinical stability.
Invasive malignancy or history of invasive malignancy other than disease under study: any other invasive malignancy from which the subject has been disease-free for more than 2 years and, in the opinion of the principal investigator and GSK Medical Monitor, will not affect the evaluation of the effects of this clinical trial treatment on currently targeted malignancy, can be included in this clinical trial; Curatively treated non-melanoma skin cancer and any carcinoma-in-situ.

Trial location(s)

Location

Status

Location

GSK Investigational Site

Chicago, Illinois, United States, 60611

Status

Study Complete

Location

GSK Investigational Site

New York, New York, United States, 10021

Status

Study Complete

Location

GSK Investigational Site

Southampton, United Kingdom, SO16 6YD

Status

Study Complete

Location

GSK Investigational Site

Sutton, Surrey, United Kingdom, SM2 5PT

Status

Study Complete

Location

GSK Investigational Site

Villejuif cedex, France, 94805

Status

Study Complete

Study documents

Protocol

Available language(s): English

Download document(s)

Statistical analysis plan

Available language(s): English

Download document(s)

If you wish to request for full study report, please contact - [email protected]

Results overview

Results posted on ClinicalTrials.gov

Recruitment status

Terminated (halted prematurely)

Actual primary completion date

2017-20-06

Actual study completion date

2017-20-06

Plain language summaries

Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.

Additional information about the trial

Additional information

Not applicable

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