Clinical Trials /

Study of a Triple Combination Therapy, DTRM-555, in Patients With R/R CLL or R/R Non-Hodgkin's Lymphomas

NCT04305444

Description:

Targeted drug therapies have greatly improved outcomes for patients with relapsed or refractory (R/R) chronic lymphocytic leukemia (CLL) and non-Hodgkin's lymphoma. However, single drug therapies have limitations, therefore, the current study is evaluating a novel oral combination of targeted drugs as a way of overcoming these limitations. This study will determine the efficacy of the triple combination therapy, DTRM-555, in patients with R/R CLL or R/R non-Hodgkin's lymphoma.

Related Conditions:
  • Chronic Lymphocytic Leukemia
  • Non-Hodgkin Lymphoma
  • Richter Syndrome
Recruiting Status:

Recruiting

Phase:

Phase 2

Trial Eligibility

Document

Title

  • Brief Title: Study of a Triple Combination Therapy, DTRM-555, in Patients With R/R CLL or R/R Non-Hodgkin's Lymphomas
  • Official Title: Phase II Expansion Cohorts Studies of a Novel Triple Combination Therapy, DTRM-555, in Patients With Relapsed/Refractory Chronic Lymphocytic Leukemia or Relapsed/Refractory Non-Hodgkin's Lymphomas

Clinical Trial IDs

  • ORG STUDY ID: DTRM-555_001
  • NCT ID: NCT04305444

Conditions

  • Relapsed Chronic Lymphocytic Leukemia
  • Refractory Chronic Lymphocytic Leukemia
  • Diffuse Large B Cell Lymphoma
  • Follicular Lymphoma
  • Richter's Transformation

Interventions

DrugSynonymsArms
DTRM-555DTRMWXHS-12, everolimus, pomalidomideDisease-specific cohorts

Purpose

Targeted drug therapies have greatly improved outcomes for patients with relapsed or refractory (R/R) chronic lymphocytic leukemia (CLL) and non-Hodgkin's lymphoma. However, single drug therapies have limitations, therefore, the current study is evaluating a novel oral combination of targeted drugs as a way of overcoming these limitations. This study will determine the efficacy of the triple combination therapy, DTRM-555, in patients with R/R CLL or R/R non-Hodgkin's lymphoma.

Detailed Description

      This study is being conducted in three parts: Phase Ia, Phase Ib and Phase II,
      disease-specific expansion cohorts. Phase Ia explored escalating doses of a monotherapy of a
      novel Bruton's Tyrosine Kinase (BTK) inhibitor, DTRMWXHS-12. Phase Ib explored two
      combination therapies, DTRM-505 (DTRMWXHS-12 and everolimus) and DTRM-555 (DTRMWXHS-12,
      everolimus and pomalidomide).

      The current Phase II study will further examine the investigational triple combination
      treatment, DTRM-555 for efficacy and safety. The study is being conducted in five
      disease-specific cohorts: Activated B-Cell (ABC) Diffuse Large B-Cell Lymphoma, Germinal
      Center B-Cell (GCB) Diffuse Large B-Cell Lymphoma, Richter's Transformation, transformed
      Follicular Lymphoma, and relapsed or refractory Chronic Lymphocytic Leukemia.

      The Primary Objective of the Phase II study is to determine the efficacy of the triple
      combination therapy, DTRM-555, in the five disease-specific cohorts. The Secondary Objectives
      are (1) to determine the safety of DTRM-555 in the cohorts and (2) to obtain the
      pharmacokinetics of DTRM-555 (i.e., DTRMWXHS-12, everolimus and pomalidomide).
    

Trial Arms

NameTypeDescriptionInterventions
Disease-specific cohortsExperimentalParticipants will be administered the oral triple-combination therapy, DTRM-555 (comprised of 200mg of DTRMWXHS-12, 5mg of everolimus and 2mg of pomalidomide), once-daily for 21 consecutive days every 28 days
  • DTRM-555

Eligibility Criteria

        Inclusion Criteria:

          -  Patients must provide written informed consent.

          -  Patients with a diagnosis of R/R CLL or other B-cell neoplasms (i.e., ABC DLBCL, GCB
             DLBCL, Richter's transformation and tFL) who have no available approved therapies, or
             patients with a diagnosis of non-Hodgkin's lymphoma, which has relapsed and/or is
             refractory to standard therapy.

             a. Patients with R/R CLL must have been exposed to Bruton's tyrosine kinase (BTK) or
             B-Cell CLL/Lymphoma 2 (BCL2) inhibitor-based therapy in prior lines of therapy but
             must not have known Cys481 resistance mutation prior to study enrollment.

          -  Age ≥ 18 years.

          -  Life expectancy greater than 12 weeks.

          -  Patients must have an Eastern Cooperative Oncology Group (ECOG) performance status of
             0 or 1.

          -  Ability to swallow and retain capsules and/or tablets.

          -  Absence of uncontrolled intercurrent illnesses, including uncontrolled infections,
             cardiac conditions, or other organ dysfunctions.

          -  If the patient consents to an optional tumor biopsy, he/she must have a tumor that can
             be safely biopsied and undergo a baseline tumor biopsy procedure, or be willing to
             provide available archival tissue collected within 6 months of signing the Informed
             Consent Form (ICF), and one post-Cycle 1 treatment biopsy.

          -  Patients must have at least one target lesion according to Lugano Classification.
             Patients with R/R CLL are exempt from this requirement.

          -  Women of child-bearing potential must have a negative serum or urine pregnancy test.

          -  Women of child-bearing potential must agree to use 2 reliable methods of contraception
             beginning 4 weeks prior to the initiation of treatment, during therapy, and for at
             least 4 weeks after the last drug administration.

          -  Men must agree to use a latex or synthetic condom during sexual contact with a
             pregnant female or a female of child-bearing potential, for the duration of the study
             and for at least 4 weeks after the last drug administration, even if they have
             undergone a successful vasectomy.

        Exclusion Criteria:

          -  Received prior systemic anticancer treatment within the following time frames:

               1. Chemotherapy, immunotherapy, radiotherapy or any other investigational therapy
                  within 21 days prior to starting study treatment.

               2. Targeted therapies within 5 biological half-lives prior to starting study
                  treatment.

          -  Patients with active infections requiring therapy are not eligible for entry into the
             study until resolution of the infection; however, patients on prophylactic
             antibiotics, antifungals or antivirals are eligible for entry into the study.

          -  Pregnant or lactating individuals.

          -  Impaired hepatic or renal function as demonstrated by any of the following laboratory
             values:

               1. Aspartate transaminase (AST) or alanine transaminase (ALT) > 2.5 x upper limit of
                  normal (ULN); for patients with liver involvement, > 5 x ULN

               2. Total bilirubin > 1.5 x ULN (Patients with a history of Gilbert's syndrome may
                  participate if total bilirubin is less than or equal to 3 x ULN and the AST/ALT
                  and alkaline phosphatase meet the protocol-specified levels for eligibility)

               3. Alkaline phosphatase > 2.5 x ULN

               4. Glomerular filtration rate < 50 mL/min, as assessed using the standard
                  methodology at the investigating center (i.e., Cockcroft-Gault), or serum
                  creatinine > 1.5 x ULN

          -  International normalized ratio (INR) > 1.5 or other evidence of impaired hepatic
             synthesis function.

          -  Absolute neutrophil count < 1.0 x 109/L or platelets < 100 x 109/L, unless due to
             disease-related bone marrow impairment as confirmed by bone marrow biopsy during
             screening or due to standard of care treatment within 2 months prior to signing of
             informed consent. Patients with bone marrow impairment will be excluded if their
             absolute neutrophil count (ANC) is < 0.5 x 109/L and platelets < 50 x 109/L.

          -  Previous allogeneic bone marrow transplant is restricted, unless transplant was
             greater than 3 months prior and there is no evidence of acute or chronic graft versus
             host disease.

          -  Central nervous system involvement with malignancy.

          -  Patients who have poorly controlled diabetes mellitus or whose glucose values cannot
             be controlled with medical treatment.

          -  Current malignancies of another type, with the exception of adequately treated in situ
             cervical cancer and basal cell skin cancer, squamous cell carcinoma of the skin or
             other malignancies with no evidence of disease for 2 years or more.

          -  Known history of human immunodeficiency virus (HIV), hepatitis B virus (HBV), or
             hepatitis C virus (HCV) infection.

          -  Documented or known bleeding disorder.

          -  Requirement for anticoagulation treatment that increases INR or activated partial
             thromboplastin time above the normal range (low molecular weight heparin and heparin
             line flush allowed).

          -  Patients requiring the use of strong CYP3A4, CYP1A2, or P-gp inhibitors.

          -  Patients with a significant cardiovascular disease or condition, including:

               1. myocardial infarction within 6 months of study entry,

               2. New York Heart Association Class III or IV heart failure,

               3. uncontrolled dysrhythmias or poorly controlled angina,

               4. history of serious ventricular arrhythmia (ventricular fibrillation or
                  ventricular tachycardia, ≥ 3 beats in a row) and/or risk factors (e.g., heart
                  failure, hypokalemia, or family history of Long QT Syndrome),

               5. baseline prolongation of QT/QTc interval (repeated demonstration of corrected QT
                  interval (QTc) ≥ 450 msec for men and 470 msec for women), and

               6. left ventricular ejection fraction (LVEF) < 45% by multiple gated acquisition
                  (MUGA) and /or echocardiogram (ECHO)
      
Maximum Eligible Age:N/A
Minimum Eligible Age:18 Years
Eligible Gender:All
Healthy Volunteers:No

Primary Outcome Measures

Measure:Complete Responses (CR) and Partial Responses (PR) with DTRM-555 in the five disease-specific cohorts
Time Frame:24 months
Safety Issue:
Description:Response in lymphoma patients will be assessed according to Lugano 2014 criteria guidelines for response assessment of Hodgkin and non-Hodgkin lymphoma. Response in CLL patients will be assessed according to International Workshop on CLL (iwCLL) 2018 criteria for treatment of CLL.

Secondary Outcome Measures

Measure:Treatment-Emergent Adverse Events (AEs) in the five disease-specific cohorts
Time Frame:24 months
Safety Issue:
Description:Percentage of participants with Treatment-Emergent Adverse Events (AEs)
Measure:Overall Response Rate (ORR) with DTRM-555 in the five disease-specific cohorts
Time Frame:6, 12 and 24 months
Safety Issue:
Description:Response in lymphoma patients will be assessed according to Lugano 2014 criteria guidelines for response assessment of Hodgkin and non-Hodgkin lymphoma. Response in CLL patients will be assessed according to iwCLL 2018 criteria for treatment of CLL.
Measure:Plasma or blood concentration versus time profiles of DTRMWXHS-12, everolimus and pomalidomide will be evaluated to determine key pharmacokinetic parameters for the three drugs
Time Frame:24 hours
Safety Issue:
Description:Plasma or blood concentration versus time profiles of DTRMWXHS-12, everolimus and pomalidomide will be evaluated to determine Area Under the Curves (AUC)
Measure:Plasma or blood concentration versus time profiles of DTRMWXHS-12, everolimus and pomalidomide will be evaluated to determine key pharmacokinetic parameters for the three drugs
Time Frame:24 hours
Safety Issue:
Description:Plasma or blood concentration versus time profiles of DTRMWXHS-12, everolimus and pomalidomide will be evaluated to determine Maximum Observed Plasma or Blood Concentrations (Cmax)
Measure:Plasma or blood concentration versus time profiles of DTRMWXHS-12, everolimus and pomalidomide will be evaluated to determine key pharmacokinetic parameters for the three drugs
Time Frame:24 hours
Safety Issue:
Description:Plasma or blood concentration versus time profiles of DTRMWXHS-12, everolimus and pomalidomide will be evaluated to determine the Times to Reach Cmax (tmax)
Measure:Plasma or blood concentration versus time profiles of DTRMWXHS-12, everolimus and pomalidomide will be evaluated to determine key pharmacokinetic parameters for the three drugs
Time Frame:24 hours
Safety Issue:
Description:Plasma or blood concentration versus time profiles of DTRMWXHS-12, everolimus and pomalidomide will be evaluated to determine Elimination Half-Lives (t1/2)

Details

Phase:Phase 2
Primary Purpose:Interventional
Overall Status:Recruiting
Lead Sponsor:Zhejiang DTRM Biopharma

Trial Keywords

  • B-Cell Lymphoma
  • Diffuse Large B Cell Lymphoma
  • Everolimus
  • Follicular Lymphoma
  • Immunosuppressive Agents
  • Leukemia
  • B-Cell Leukemia
  • Chronic Lymphocytic Leukemia
  • Lymphatic Diseases
  • Lymphoma
  • Malignant Lymphoma
  • Non-Hodgkin Lymphoma
  • Lymphoproliferative Disorders
  • Neoplasms
  • Tyrosine Protein Kinase
  • Bruton's Tyrosine Kinase Inhibitor
  • Pomalidomide

Last Updated

March 10, 2020