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First Time in Humans (FTIH) Study of GSK3368715 in Subjects With Solid Tumors and Diffuse Large B-cell Lymphoma (DLBCL)

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ClinicalTrials.gov Identifier: NCT03666988
Recruitment Status : Recruiting
First Posted : September 12, 2018
Last Update Posted : October 29, 2019
Sponsor:
Information provided by (Responsible Party):
GlaxoSmithKline

Brief Summary:
Arginine methylation mediated by protein arginine methyl-transferases (PRMTs) is an important post-translational modification of proteins involved in a diverse range of cellular processes. Misregulation and overexpression of PRMT1 (a type I PRMT) has been associated with a number of solid and hematopoietic cancers. GSK3368715 leads to inhibition of tumor cell growth across tumor types with cytotoxic response observed in lymphoma, acute myeloid leukemia (AML) and a subset of solid tumor cell lines. This study will assess the safety, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary clinical activity of GSK33368715 in subjects with relapsed/refractory DLBCL and selected solid tumors with frequent methyl-thioadenosine phosphorylase (MTAP)-deficiency. The study will consist of two parts. In Part 1 (Dose Escalation) escalating doses of GSK3368715 will be evaluated and recommended phase 2 dose (RP2D) will be established in subjects with selected solid relapsed/refractory tumors. In Part 2 (Dose Expansion), this RP2D will be further investigated in two expansion cohorts; subjects with DLBCL (Expansion Cohort 2A) and relapsed/refractory solid tumors including pancreatic, bladder, and non-small cell lung cancer (NSCLC)(Expansion Cohort 2B). The study includes a screening period, an intervention period and follow up. Approximately 40 subjects will be enrolled in Part 1 and 141 will be enrolled in Part 2.

Condition or disease Intervention/treatment Phase
Neoplasms Drug: GSK3368715 Phase 1

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 215 participants
Allocation: Non-Randomized
Intervention Model: Sequential Assignment
Intervention Model Description: Eligible subjects will receive sequential doses of GSK3368715, administered orally once daily in Part 1 of the study and in Part 2, subjects will receive RP2D determined in Part 1.
Masking: None (Open Label)
Masking Description: This will be an open-label study. Hence, masking will not be performed.
Primary Purpose: Treatment
Official Title: A Phase I, Open-label, Dose-escalation Study to Investigate the Safety, Pharmacokinetics, Pharmacodynamics and Clinical Activity of GSK3368715 in Participants With Solid Tumors and DLBCL
Actual Study Start Date : October 22, 2018
Estimated Primary Completion Date : June 18, 2022
Estimated Study Completion Date : June 18, 2022


Arm Intervention/treatment
Experimental: Part 1: GSK3368715 dose escalation cohort
Eligible subjects with solid relapsed/refractory tumors will receive escalating doses of GSK3368715 at a starting dose of 50 mg, administered orally once daily.
Drug: GSK3368715
GSK3368715 will be available with dosing strengths of 25 mg, 100 mg and 250 mg to be administered once daily as an oral capsule.

Experimental: Part 1: GSK3368715 PK/PD/Metabolite/Biomarker cohort
Additional subjects in Part 1, treated at or close to the expected the maximum tolerated dose (MTD)/RP2D, will be evaluated for metabolic and biomarker profiling. Subjects may be enrolled into this cohort(s) even after MTD/RP2D has been identified and Part 2 has been initiated.
Drug: GSK3368715
GSK3368715 will be available with dosing strengths of 25 mg, 100 mg and 250 mg to be administered once daily as an oral capsule.

Experimental: Part 2:GSK3368715 dose expansion cohort - DLBCL subjects
Eligible subjects with relapsed/refractory DLBCL will receive RP2D of GSK3368715 established during Part 1, administered orally once daily.
Drug: GSK3368715
GSK3368715 will be available with dosing strengths of 25 mg, 100 mg and 250 mg to be administered once daily as an oral capsule.

Experimental: Part 2:GSK3368715 dose expansion cohort - solid tumor subjects
Eligible subjects with relapsed/refractory solid tumors (pancreas cancer, NSCLC, and bladder cancer) will receive RP2D of GSK3368715 established during Part 1, administered orally once daily.
Drug: GSK3368715
GSK3368715 will be available with dosing strengths of 25 mg, 100 mg and 250 mg to be administered once daily as an oral capsule.




Primary Outcome Measures :
  1. Part 1: Number of subjects with dose limiting toxicity (DLT) [ Time Frame: Up to 21 days ]
    An adverse event (AE) is considered to be a DLT if the event is considered by the investigator to be clinically relevant and attributed (definitely, probably or possibly) to the study intervention during the first 21 days of intervention and meets DLT criteria for non-hematologic and hematologic Toxicities.

  2. Part 1: Number of subjects with AEs and serious AEs (SAEs) [ Time Frame: Up to 3.9 years ]
    An AE is any untoward medical occurrence in a clinical study subject, temporally associated with the use of a study intervention, whether or not considered related to the study intervention. Any untoward event resulting in death, life threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent disability/incapacity, congenital anomaly/birth defect or any other situation according to medical or scientific judgment will be categorized as serious adverse event (SAE).

  3. Part 1: Number of subjects with AEs by maximum grade [ Time Frame: Up to 3.9 years ]
    An AE is any untoward medical occurrence in a clinical study subject, temporally associated with the use of a study intervention, whether or not considered related to the study intervention. AEs will be graded using Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 (V5.0).

  4. Part 2: Objective response rate (ORR) [ Time Frame: Up to 3.9 years ]
    ORR is defined as the percentage of subjects with a confirmed complete response (CR) or a partial response (PR). Subjects with solid tumor will be assessed per Response Criteria for Solid Tumors (RECIST) 1.1 and DLBCL subjects will be assessed per Lugano Criteria.


Secondary Outcome Measures :
  1. Part 1: Best overall response [ Time Frame: Up to 3.9 years ]
    The best overall response is the best response recorded from the start of the intervention until disease progression/initiation of new anti-cancer therapy and will be determined based on the investigators assessment of response at each time point.

  2. Part 1: Maximum observed plasma concentration (Cmax) following administration of GSK3368715 [ Time Frame: Pre-dose,15,30 minutes(min),1,1.5,2,3,4,6,8,12,24,48,72hours(h) post-dose (Day1) of each cycle; Pre-dose,30 min,1,2, 3,4,6,8,12,24 h post-dose on Day15 of each cycle; Pre-dose on Days 22,28 and at every 4 weeks from Cycle2 (Each cycle will be of 21days) ]
    Cmax of GSK3368715 is to be derived from the PK samples collected.

  3. Part 1: Time to reach Cmax (Tmax) following administration of GSK3368715 [ Time Frame: Pre-dose,15,30 min, 1,1.5,2,3,4,6,8,12,24,48,72 h post-dose (Day1) of each cycle; Pre-dose,30 min,1,2, 3,4,6,8,12,24 h post-dose on Day15 of each cycle; Pre-dose on Days 22,28 and at every 4 weeks from Cycle2 (Each cycle will be of 21days) ]
    Tmax of GSK3368715 is to be derived from the PK samples collected.

  4. Part 1: Area under the concentration time curve from time zero to last time of quantifiable concentration (AUC [0-t]) following administration of GSK3368715 [ Time Frame: Pre-dose,15,30 min, 1,1.5,2,3,4,6,8,12,24,48,72 h post-dose (Day1) of each cycle; Pre-dose,30 min,1,2, 3,4,6,8,12,24 h post-dose on Day15 of each cycle; Pre-dose on Days 22,28 and at every 4 weeks from Cycle2 (Each cycle will be of 21days) ]
    AUC(0-t) of GSK3368715 is to be derived from the PK samples collected.

  5. Part 1: AUC from time zero extrapolated to infinite time (AUC [0-infinity]) following single dose administration of GSK3368715 [ Time Frame: Pre-dose, 15, 30 min, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 48, 72 h post-dose on Day 1 of each cycle (Each cycle will be of 21 days) ]
    AUC(0-infinity) of GSK3368715 is to be derived from the PK samples collected.

  6. Part 1: Area under the concentration-time curve over the dosing interval (AUC [0-tau]) following repeat dose administration of GSK3368715 [ Time Frame: Pre-dose, 15, 30 min, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 48, 72 h post-dose on Day 1; Pre-dose, 30 min,1,2, 3,4,6,8,12,24 h post-dose on Day 15 of each cycle;Pre-dose on Days 22,28 and at every 4 weeks from Cycle 2 (Each cycle will be of 21 days) ]
    AUC(0-tau) of GSK3368715 is to be derived from the PK samples collected.

  7. Part 1: Trough concentration (Ctau) following repeat dose administration of GSK3368715 [ Time Frame: Pre-dose on Day 8 and Day 15;Pre-dose on Days 22,28 and at every 4 weeks from Cycle 2 (Each cycle will be of 21 days) ]
    Ctau of GSK3368715 is to be derived from the PK samples collected.

  8. Part 1: Time invariance ratio following administration of GSK3368715 [ Time Frame: Pre-dose, 15, 30 min, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 48, 72 h post-dose on Day 1; Pre-dose, 30 min, 1, 2, 3, 4, 6, 8, 12, 24 h post-dose on Day 15 of each cycle (Each cycle will be of 21 days) ]
    Time invariance ratio of GSK3368715 is to be derived from the PK samples collected wherever data permits.

  9. Part 1: Accumulation ratio following administration of GSK3368715 [ Time Frame: Pre-dose, 15, 30 min, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 48, 72 h post-dose on Day 1; Pre-dose, 30 min, 1, 2, 3, 4, 6, 8, 12, 24 h post-dose on Day 15 of each cycle (Each cycle will be of 21 days) ]
    Accumulation ratio of GSK3368715 is to be derived from the PK samples collected wherever data permits.

  10. Part 2: Number of subjects with AEs and SAEs [ Time Frame: Up to 3.9 years ]
    An AE is any untoward medical occurrence in a clinical study subject, temporally associated with the use of a study intervention, whether or not considered related to the study intervention. Any untoward event resulting in death, life threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent disability/incapacity, congenital anomaly/birth defect or any other situation according to medical or scientific judgment will be categorized as SAE.

  11. Part 2: Number of subjects with AEs by maximum grade [ Time Frame: Up to 3.9 years ]
    An AE is any untoward medical occurrence in a clinical study subject, temporally associated with the use of a study intervention, whether or not considered related to the study intervention. AEs will be graded using CTCAE V5.0.

  12. Part 2: Progression-free survival (PFS) [ Time Frame: Up to 3.9 years ]
    PFS is defined as the time from the first dose of study intervention to disease progression or death due to any cause, whichever occurs earlier.

  13. Part 2: Cmax following administration of GSK3368715 [ Time Frame: Pre-dose, 15, 30 min, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 48, 72 h post-dose (Day1) of each cycle; Pre-dose, 30 min,1,2, 3,4,6,8,12,24 h post-dose on Day15 of each cycle; Pre-dose on Days 22,28 and at every 4 weeks from Cycle 2 (Each cycle will be of 21 days) ]
    Cmax of GSK3368715 is to be derived from the PK samples collected.

  14. Part 2: Tmax following administration of GSK3368715 [ Time Frame: Pre-dose, 15, 30 min, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 48, 72 h post-dose (Day1) of each cycle; Pre-dose, 30 min,1,2, 3,4,6,8,12,24 h post-dose on Day15 of each cycle; Pre-dose on Days 22,28 and at every 4 weeks from Cycle 2 (Each cycle will be of 21 days) ]
    Tmax of GSK3368715 is to be derived from the PK samples collected.

  15. Part 2: AUC (0-t) following administration of GSK3368715 [ Time Frame: Pre-dose,15,30 min,1, 1.5, 2,3,4,6,8,12,24,48,72 h post-dose (Day1) of each cycle; Pre-dose, 30 min,1,2, 3,4,6,8,12,24 h post-dose on Day 15 of each cycle; Pre-dose on Days 22,28 and at every 4 weeks from Cycle 2 (Each cycle will be of 21 days) ]
    AUC(0-t) of GSK3368715 is to be derived from the PK samples collected.

  16. Part 2: AUC (0-infinity) following single dose administration of GSK3368715 [ Time Frame: Pre-dose, 15, 30 min, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 48, 72 h post-dose on Day 1 of each cycle (Each cycle will be of 21 days) ]
    AUC (0-infinity) of GSK3368715 is to be derived from the PK samples collected.

  17. Part 2: AUC (0-tau) following repeat dose administration of GSK3368715 [ Time Frame: Pre-dose, 15, 30 min, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 48, 72 h post-dose on Day 1; Pre-dose, 30 min,1,2, 3,4,6,8,12,24 h post-dose on Day 15 of each cycle; Pre-dose on Days 22,28 and at every 4 weeks from Cycle 2 (Each cycle will be of 21 days) ]
    AUC (0-tau) of GSK3368715 is to be derived from the PK samples collected.

  18. Part 2: Ctau following repeat dose administration of GSK3368715 [ Time Frame: Pre-dose, 15, 30 min, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 48, 72 h post-dose on Day 1; Pre-dose, 30 min,1,2, 3,4,6,8,12,24 h post-dose on Day 15 of each cycle; Pre-dose on Days 22,28 and at every 4 weeks from Cycle 2 (Each cycle will be of 21 days) ]
    Ctau of GSK3368715 is to be derived from the PK samples collected.

  19. Part 2: Time invariance ratio following administration of GSK3368715 [ Time Frame: Pre-dose, 15, 30 min, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 48, 72 h post-dose on Day 1; Pre-dose, 30 min, 1, 2, 3, 4, 6, 8, 12, 24 h post-dose on Day 15 of each cycle (Each cycle will be of 21 days) ]
    Time invariance ratio of GSK3368715 is to be derived from the PK samples collected wherever data permits.

  20. Part 2: Accumulation ratio following administration of GSK3368715 [ Time Frame: Pre-dose, 15, 30 min, 1, 1.5, 2, 3, 4, 6, 8, 12, 24, 48, 72 h post-dose on Day 1; Pre-dose, 30 min, 1, 2, 3, 4, 6, 8, 12, 24 h post-dose on Day 15 of each cycle (Each cycle will be of 21 days) ]
    Accumulation ratio of GSK3368715 is to be derived from the PK samples collected wherever data permits.



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria: - Subject must be >=18 to years of age inclusive, at the time of signing the informed consent. - Diagnosis of one of the following; Part 1 (Dose Escalation): Histologically- or cytological-confirmed diagnosis of solid tumor malignancy that is metastatic or non-resectable; have received all standard treatment options or are no longer eligible for additional standard treatment options. Evaluable disease that may be measured directly by the size of the tumor or can be evaluated by other methods. Availability of a biopsy of the tumor tissue obtained at any time from the initial diagnosis to study entry. Although a fresh biopsy, which is obtained during screening, is preferred, archival tumor specimen is acceptable if it is not feasible to obtain a fresh biopsy. For subjects in the PK/PD cohort, a fresh biopsy and consent for one on treatment biopsy are required for enrollment. Part 2 (Dose Expansion): Cohort 2A & 2B: The availability of archival tumor tissue, or willingness to undergo a fresh biopsy to determine MTAP status (any archival tumor specimen must have been obtained within 6 months prior to starting study drug unless approved by the study Medical Monitor). Local MTAP or Cyclin Dependent Kinase Inhibitor 2A (CDKN2A) results are acceptable for enrollment, but must be confirmed through central laboratory testing. . Cohort 2A: Histologically- or cytological-confirmed diagnosis of DLBCL; relapse or refractory disease after at least 1 but not more than 4 lines of prior therapy; at least 1 measurable site of disease according to the Lugano Classification. The site of disease must be greater than 1.5 centimeter (cm) in the long axis regardless of short axis measurement or greater than 1.0 cm in the short axis regardless of long axis measurement, and clearly measurable in 2 perpendicular dimensions. Cohort 2B: Pancreatic Cancer: Histologically or cytologically confirmed adenocarcinoma of the pancreas; unresectable, locally advanced (Stage III), or metastatic (Stage IV) disease; relapsed or refractory disease after at least 1 prior line of approved, systemic therapy; at least 1 measurable tumor lesion per RECIST 1.1. NSCLC: histologically or cytologically confirmed NSCLC; stage IV disease; tested for presence of echinoderm microtubule-associated protein-like 4- anaplastic lymphoma kinase (EML4-ALK) rearrangement; received at least 2 prior lines of approved, systemic therapy, of which 1 therapy has to be a platinum containing regimen or failed a first-line platinum-containing regimen in combination with an anti- progressive disease (PD1) monocloncal antibody and refused a second-line regimen despite being informed about the different therapeutic options and their specific clinical benefit by the investigator; the content of this informed consent discussion including the therapeutic options reviewed by the investigator need to be documented and the subject needs to sign a specific consent form; at least 1 measurable tumor lesion per RECIST 1.1. Transitional cell carcinoma of the Urothelium: histologically or cytologically confirmed transitional cell carcinoma (TCC) of the urothelium (urinary bladder, urethra, ureter or renal pelvis) including mixed pathology with predominantly (that is [i.e.], > 50 percent of the histopathology sample) TCC with the exception of neuroendocrine or small cell carcinoma; unresectable, locally advanced (T4b) or metastatic (lymph node or visceral) disease; relapsed or refractory disease after at least 1 prior line of approved systemic therapy; at least 1 measurable tumor lesion per RECIST 1.1. - Adequate organ function as defined by: Absolute neutrophil count (ANC) with a laboratory value of >=1.5 times 10^9 per liter (L); Hemoglobin with a laboratory value of >=9 grams per deciliter (g/dL) for solid malignancy and >=8 g/dL for Non-Hodgkin's lymphoma; Platelets with a laboratory value of >=100 times 10^9/ L; prothrombin time/ International Normalization Ratio (PT/INR) and partial thromboplastin time (PTT) with a laboratory value of <=1.5 times upper limit of normal (ULN), unless subject is receiving systemic anticoagulation (Hematologic); Albumin with a laboratory value of >=2 g/dL, total bilirubin with a laboratory value of <=1.5 times ULN, alanine aminotransferase (ALT) with a laboratory value of <=2.5 times ULN (Part 1 and 2) or <5 times ULN (Part 2 only) is acceptable for subjects with documented liver metastases/tumor infiltration (Hepatic); calculated creatinine clearance by Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation or measured from 24 h urine with a laboratory value of >= 50 milliliters per min (mL/min) (Renal); Ejection fraction with a laboratory value of >=Lower limit of normal (LLN) by echocardiogram (minimum of 50 percent)/ multigated (radionuclide) angiogram (MUGA), Electrocardiogram (ECG): corrected QT (QTc) interval using Fridericia's formula (QTcF) with a laboratory value of <450 milliseconds (msec) (Cardiac). - Eastern cooperative oncology group (ECOG) performance status of 0 or 1. - Able to swallow and retain orally-administered medication. - A female subject is eligible to participate if she is not pregnant or breastfeeding, and at least one of the following conditions applies; is not a woman of childbearing potential (WOCBP) or is a WOCBP and using a contraceptive method that is highly effective, with a failure rate of <1 percent, during the intervention period and for at least 120 days, corresponding to the time needed to eliminate any study intervention(s) (example given [e.g.], 5 terminal half-lives) after the last dose of study intervention. The investigator should evaluate the effectiveness of the contraceptive method in relationship to the first dose of study intervention. A WOCBP must have a negative highly sensitive pregnancy test (urine as required by local regulations) within 7 days before the first dose of study intervention. The investigator is responsible for review of medical history, menstrual history, and recent sexual activity to decrease the risk for inclusion of a woman with an early undetected pregnancy. Male subjects are eligible to participate if they agree to the following during the intervention period and for at least 100 days, corresponding to time needed to eliminate study intervention(s) (e.g., 5 terminal half-lives) plus 90 days after the last dose of study intervention: Refrain from donating sperm plus either: Be abstinent from heterosexual or homosexual intercourse as their preferred and usual lifestyle (abstinent on a long term and persistent basis) and agree to remain abstinent or must agree to use contraception/barrier as detailed below; agree to use a male condom and should also be advised of the benefit for a female partner to use a highly effective method of contraception as a condom may break or leak when having sexual intercourse with a woman of childbearing potential who is not currently pregnant; agree to use male condom when engaging in any activity that allows for passage of ejaculate to another person. - Capable of giving signed informed consent.

Exclusion Criteria: - History of malignancy other than the disease under study. Subjects who have been disease-free for 5 years, or subjects with a history of completely resected non-melanoma skin cancer or successfully treated in situ carcinoma are eligible. Subjects with second malignancies that are indolent or definitively treated may be enrolled even if less than 5 years have elapsed since treatment. - Primary central nervous system (CNS) tumors, Glioblastoma multiforme (GBM), symptomatic or untreated leptomeningeal or brain metastases or spinal cord compression. Subjects previously treated for these conditions that have had stable CNS disease (verified with consecutive imaging studies) for >1 months, are asymptomatic and off corticosteroids, or are on stable dose of corticosteroids for at least 1 month prior to study Day 1 are permitted. Stability of brain metastases must be confirmed with imaging. Subjects treated with gamma knife therapy can be enrolled 2 weeks post-procedure as long as there are no post-procedure complications/they are stable. - Any severe or uncontrolled systemic diseases (e.g., unstable or uncompensated respiratory, hepatic, renal, cardiac disease, or clinically significant bleeding episodes, or active infection). - Any serious and/or unstable pre-existing medical, psychiatric disorder, or other conditions that could interfere with subject's safety, obtaining informed consent or compliance to the study procedures, in the opinion of the Investigator. - Any clinically significant gastrointestinal (GI) abnormalities that may alter absorption such as malabsorption syndrome or major resection of the stomach and/or bowels. - History of known human immunodeficiency virus (HIV) infection or positive HIV test result at screening. - Presence of hepatitis B surface antigen (HBsAg) or positive hepatitis C antibody test result at screening to first dose of study intervention. - Any of the following cardiac abnormalities: Uncontrolled high blood pressure; any history of coronary artery disease, including acute coronary syndromes, myocardial infarction, unstable angina, and history of coronary angioplasty, or stenting; presence of a cardiac pacemaker or implanted defibrillator; atrioventricular (AV)-block (asymptomatic 2nd degree Type II or 3rd degree and any degreeAV block if related to heart disease or if symptomatic), right bundle branch block (RBBB), left bundle branch block (LBBB), and any fasicular hemiblocks; A QRS interval at Screening or Baseline >100 msec; subjects with any symptomatic or sustained arrhythmias (past or present), including but not limited to: Atrial fibrillation, Atrial flutter, Ventricular tachycardia, Ventricular fibrillation, Supraventricular tachycardia; Current or past congestive heart failure; Evidence of a left ventricular ejection fraction below the institutional lower limit of normal on Screening echocardiogram; Evidence of significant structural heart disease on echocardiography at Screening (including any valvular disease greater than "mild" in severity); Cardiac troponin > upper limit of the reference range at Screening. - Treatment with any local or systemic anti-neoplastic therapy or investigational anticancer agent within 14 days or 4 half-lives, whichever is longer, up to a maximum wash-out period of 28 days prior to initiation of study drug administration. Anti-androgen therapies for prostate cancer, such as bicalutamide, must be stopped 28 days prior to first dose of GSK3368715. Second-line hormone therapies such as enzalutamide or abiraterone should be stopped 14 days prior to enrolment. Subjects with prostate cancer may remain on luteinizing hormone-releasing hormone (LHRH) agonists or antagonists and/or low-dose prednisone or prednisolone (up to 10 milligrams per day [mg/day]). Nitrosureas and mitomycin C must be stopped within 42 days prior to first dose of GSK3368715. - Allogeneic hematopoietic stem-cell transplantation. - Toxicities from previous anti-cancer therapies have not resolved to Baseline or National Cancer Institute (NCI) CTCAE V5.0. <=Grade 1 (except fatigue and alopecia [permissible at any grade] and peripheral neuropathy [which must be <= Grade 2]) at the time of starting study intervention. - Major surgery (i.e. requiring general anesthesia) within 3 weeks before screening, or not fully recovered from major surgery, or major surgery planned during study participation. Planned surgical procedures to be conducted under local anesthesia are allowed. - Prior organ transplantation. - Concurrent anti-coagulation therapy. Treatment with low-molecular heparin is allowed. - Current use of a prohibited medication or planned use of any forbidden medications during intervention with GSK3368715. - History of sensitivity to any of the study medications, or components thereof or a history of drug or other allergy that, in the opinion of the investigator or Medical Monitor, contraindicates their participation.


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03666988


Contacts
Layout table for location contacts
Contact: US GSK Clinical Trials Call Center 877-379-3718 GSKClinicalSupportHD@gsk.com
Contact: EU GSK Clinical Trials Call Center +44 (0) 20 89904466 GSKClinicalSupportHD@gsk.com

Locations
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United States, California
GSK Investigational Site Recruiting
Los Angeles, California, United States, 90033
Contact: US GSK Clinical Trials Call Center    877-379-3718    GSKClinicalSupportHD@gsk.com   
Contact: EU GSK Clinical Trials Call Centre    +44 (0) 20 8990 4466    GSKClinicalSupportHD@gsk.com   
Principal Investigator: Anthony El-Khoueiry         
GSK Investigational Site Recruiting
Newport Beach, California, United States, 92663
Contact: US GSK Clinical Trials Call Center    877-379-3718    GSKClinicalSupportHD@gsk.com   
Contact: EU GSK Clinical Trials Call Centre    +44 (0) 20 8990 4466    GSKClinicalSupportHD@gsk.com   
Principal Investigator: Anthony El-Khoueiry         
United States, Massachusetts
GSK Investigational Site Recruiting
Boston, Massachusetts, United States, 02215
Contact: US GSK Clinical Trials Call Center    877-379-3718    GSKClinicalSupportHD@gsk.com   
Contact: EU GSK Clinical Trials Call Centre    +44 (0) 20 8990 4466    GSKClinicalSupportHD@gsk.com   
Principal Investigator: Gerburg Wulf         
United States, New York
GSK Investigational Site Recruiting
New York, New York, United States, 10016
Contact: US GSK Clinical Trials Call Center    877-379-3718    GSKClinicalSupportHD@gsk.com   
Contact: EU GSK Clinical Trials Call Centre    +44 (0) 20 8990 4466    GSKClinicalSupportHD@gsk.com   
Principal Investigator: Daniel Cho         
United States, Pennsylvania
GSK Investigational Site Recruiting
Philadelphia, Pennsylvania, United States, 19104
Contact: US GSK Clinical Trials Call Center    877-379-3718    GSKClinicalSupportHD@gsk.com   
Contact: EU GSK Clinical Trials Call Centre    +44 (0) 20 8990 4466    GSKClinicalSupportHD@gsk.com   
Principal Investigator: Peter O'Dwyer         
United States, Texas
GSK Investigational Site Recruiting
Houston, Texas, United States, 77030
Contact: US GSK Clinical Trials Call Center    877-379-3718    GSKClinicalSupportHD@gsk.com   
Contact: EU GSK Clinical Trials Call Centre    +44 (0) 20 8990 4466    GSKClinicalSupportHD@gsk.com   
Principal Investigator: Jordi Ahnert         
United States, Utah
GSK Investigational Site Recruiting
Salt Lake City, Utah, United States, 84112
Contact: US GSK Clinical Trials Call Center    877-379-3718    GSKClinicalSupportHD@gsk.com   
Contact: EU GSK Clinical Trials Call Centre    +44 (0) 20 8990 4466    GSKClinicalSupportHD@gsk.com   
Principal Investigator: Ignacio Garrido-Laguna         
Australia, Victoria
GSK Investigational Site Recruiting
Melbourne, Victoria, Australia, 3000
Contact: US GSK Clinical Trials Call Center    877-379-3718    GSKClinicalSupportHD@gsk.com   
Contact: EU GSK Clinical Trials Call Centre    +44 (0) 20 8990 4466    GSKClinicalSupportHD@gsk.com   
Principal Investigator: Ben Tran         
Canada, Ontario
GSK Investigational Site Recruiting
Toronto, Ontario, Canada, M5G 2M9
Contact: US GSK Clinical Trials Call Center    877-379-3718    GSKClinicalSupportHD@gsk.com   
Contact: EU GSK Clinical Trials Call Centre    +44 (0) 20 8990 4466    GSKClinicalSupportHD@gsk.com   
Principal Investigator: Albiruni Ryan Abdul Razak         
Sponsors and Collaborators
GlaxoSmithKline
Investigators
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Study Director: GSK Clinical Trials GlaxoSmithKline

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Responsible Party: GlaxoSmithKline
ClinicalTrials.gov Identifier: NCT03666988     History of Changes
Other Study ID Numbers: 207675
2018-001629-20 ( EudraCT Number )
First Posted: September 12, 2018    Key Record Dates
Last Update Posted: October 29, 2019
Last Verified: October 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
Plan Description: IPD for this study will be made available via the Clinical Study Data Request site.
Supporting Materials: Study Protocol
Statistical Analysis Plan (SAP)
Informed Consent Form (ICF)
Clinical Study Report (CSR)
Time Frame: IPD will be made available within 6 months of publishing the results of the primary endpoints of the study.
Access Criteria: Access is provided after a research proposal is submitted and has received approval from the Independent Review Panel and after a Data Sharing Agreement is in place. Access is provided for an initial period of 12 months but an extension can be granted, when justified, for up to another 12 months.
URL: http://clinicalstudydatarequest.com

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by GlaxoSmithKline:
Dose-escalation
First time in humans
Solid tumors
GSK3368715
Diffuse Large B-Cell Lymphoma