Molecular Templates, Inc.

MT-3724 With Lenalidomide for Relapsed/Refractory Diffuse Large B Cell Non-Hodgkin's Lymphoma

Trial Summary

Official Title

A Phase 2a Open-label Study to Investigate Safety and Tolerability (Including the Maximum Tolerated Dose), Efficacy, Pharmacokinetics, Pharmacodynamics and Immunogenicity of MT-3724 in Combination With Lenalidomide in Subjects With Relapsed or Refractory B-Cell Non-Hodgkin Lymphoma

Status

Active, not recruiting

Condition

Non-hodgkin Lymphoma

Actual Start Date

April 8, 2019

Estimated Primary Completion Date

December 17, 2020

About the Trial

PK,PD, Safety and Tolerability of Multiple Dose Regimens of MT-3724 With Lenalidomide for the Treatment of Patients With Relapsed/Refractory B-Cell Non-Hodgkin's Lymphoma (MT-3724_NHL_003)

This is a multi-center, open-label two-part study evaluating the safety and tolerability of MT-3724 in combination with Lenalidomide in relapsed or refractory CD20 positive B-cell Lymphoma patients.

Part 1: (MT-3724 Dose Escalation) Define the maximum tolerated dose (MTD) of MT-3724 in combination with standard treatment of Lenalidomide

Part 2: (MTD Expansion Cohort) Confirm the safety and tolerability of the MTD of MT-3724 from Part 1 in the MTD Expansion Cohort, where MT-3724 will be given at the MTD in combination with Lenalidomide. In addition, the PK, PD, immunogenicity and tumor response at the MTD of MT-3724 in combination with Lenalidomide will be more thoroughly evaluated in Part 2.

It is anticipated that up to 64 patients will be enrolled. Treatment will continue until disease progression, withdrawal of consent or any other reason.

Detailed Info

Brief Summary

The purpose of this study is to evaluate the safety and tolerability of MT-3724 in combination with Lenalidomide in subjects with relapsed or refractory B-Cell NHL.

Study Phase

Phase 2

Estimated Enrollment

64

Estimated Primary Completion Date

December 17, 2020

Study Type

Interventional

Interventions

  • Drug: MT-3724

Sponsor

Molecular Templates, Inc.

Inclusion Criteria

Gender

Male & Female

Age

18 Years to 101 Years

  • Subjects must meet ALL the following criteria to be eligible for the study.

    1. Be adequately informed about the study and fully consent to participation as demonstrated by signing the written informed consent form before any screening procedure.
    2. Men or Women , age 18 years or older Have relapsed or refractory B-cell NHL that, in the investigator's opinion, could benefit from MT-3724+LEN therapy.
    3. At least one histology documented relapse of NHL by:

      1. Bone marrow biopsy (FNA is not acceptable)
      2. Excisional lymph node biopsy or
      3. Core biopsy of any involved organ (FNA not acceptable)
      4. CD20-positive histology must have been confirmed at any time during NHL disease course and documented in the medical history.
      5. If no histology is available after any relapse the investigator can consult the medical monitor to discuss if the patient can be included
    4. All subtypes of B-cell NHL may be considered for Part 1 (MT-3724 dose escalation). Only histologically documented DLBCL (including mixed histology) may be considered for Part 2 (expansion cohort)
    5. Have received all available approved therapies for NHL. Those subjects who are ineligible for approved therapies in the opinion of the investigator, or have refused such therapies, will be eligible.
    6. Have measurable disease by Lugano Classification for NHL (see Appendix 4):

      1. >1.5 cm longest diameter (LDi) for lymph nodes
      2. >1.0 cm LDi for extra nodal disease.
    7. Eastern Cooperative Oncology Group (ECOG) performance score of ≤2
    8. Have adequate bone marrow function, as determined by all the following:

      1. Absolute neutrophil count (ANC) ≥1,000/mm³
      2. Platelet count ≥50,000 mm³
    9. Have adequate kidney function, assessed by the estimated glomerular filtration rate (eGFR) ≥60 mL/min calculated by the CPK-EPI equation.

      a. At the investigator's discretion, the eGFR result <60 mL/min may be verified by measurement of creatinine clearance (CLcr) based on the 24-hour urine collection. Subjects with CLcr ≥60 mL/min will be eligible irrespective of the eGFR result.

    10. Have adequate hepatic function, as determined by:

      1. Total bilirubin ≤1.5 x ULN, or ≤3 x ULN for subjects with Gilbert's Syndrome) and
      2. AST ≤3 x ULN and
      3. ALT ≤3 x ULN
    11. Have adequate coagulation, as determined by:

      1. INR or PT ≤1.5 x ULN
      2. PTT ≤1.5 x ULN
    12. Have adequate serum albumin, as determined by:

      a. Albumin ≥ 3.0 g/dL

    13. Women of reproductive potential must have a negative pregnancy test on 2 occasions during the screening period (within 10-14 days and within 24 hours before the start of treatment). Women not of reproductive potential are female subjects who are postmenopausal or permanently sterilized (e.g., hysterectomy, bilateral salpingectomy).
    14. Males must agree to always use a latex or synthetic condom during any sexual contact with females of reproductive potential while taking LEN and for up to 4 weeks after discontinuing LEN, even if they have undergone a successful vasectomy. Male patients taking LEN must not donate sperm.
    15. Subjects of reproductive potential and their partners must agree to either to abstain continuously from heterosexual intercourse or to use 2 methods of reliable birth control simultaneously to begin 4 weeks prior to initiating treatment with LEN until 28 days after the last dose of MT-3724 or LEN. The investigator or a designated associate should advise the subject how to achieve adequate contraception. The following birth control methods may be considered: one highly effective form of contraception - tubal ligation, IUD, hormonal (birth control pills, injections, hormonal patches, vaginal rings, or implants), or partner's vasectomy, and one additional effective contraceptive method - male latex or synthetic condom, diaphragm, or cervical cap.

Exclusion Criteria

  • Subjects who meet any of the following criteria must be excluded from the study.

Medical and surgical history

  1. History or current evidence of neoplastic disease that is histologically distinct from NHL, except cervical carcinoma in situ, superficial noninvasive bladder tumors, curatively treated Stage I-II non-melanoma skin cancer or any previous cancer curatively treated >2 years before the start of treatment.
  2. Current evidence of new or growing brain or spinal metastases during screening. Subjects with known brain or spinal metastases may be eligible if they

    1. Had radiotherapy or another appropriate therapy for the brain or spinal metastases
    2. Have no neurological symptoms (excluding Grade ≤2 neuropathy)
    3. Have stable brain or spinal disease on the CT or MRI scan within 1 month of enrollment
    4. Do not require chronic steroid therapy
  3. History of allogeneic hematopoietic stem cell transplant within 180 days before the start of treatment.
  4. Current evidence of acute or chronic Graft versus Host Disease.
  5. Current evidence of CTCAE Grade >1 toxicity (except for hair loss, and those toxicities listed in other eligibility criteria) before the start of treatment.
  6. Current evidence of incomplete recovery from surgery before the start of treatment, or planned surgery at any time during the study until the EoT Visit, except minor elective interventions deemed acceptable by the investigator.
  7. History or current evidence of significant (CTCAE Grade ≥2) infection or wound within 4 weeks before the start of treatment.
  8. History or current evidence of significant cardiovascular disease including, but not limited to the following conditions:

    1. Unstable angina (symptoms of angina at rest) or new-onset angina within ≤3 months before the start of treatment.
    2. Arterial thrombosis or pulmonary embolism within ≤3 months before the start of treatment.
    3. Myocardial infarction or stroke within ≤3 months before the start of treatment.
    4. Pericarditis (any CTCAE grade), pericardial effusion (CTCAE Grade ≥2), non malignant pleural effusion (CTCAE Grade ≥2) or malignant pleural effusion (CTCAE Grade ≥3).
    5. Congestive heart failure (NYHA Class III or IV) at screening or LVEF <45%, assessed by Echo or MUGA scan within 1 month before starting study treatment. (Echo or MUGA scan performed within 6 months before screening and at least 28 days after the last cancer therapy is acceptable provided the subject has not received any potential cardiotoxic agents).
    6. Cardiac arrhythmia requiring anti-arrhythmic therapy at screening. Subjects receiving digoxin, calcium channel blockers, or beta-adrenergic blockers are eligible at the investigator's discretion after consultation with Medical Monitor if the dose has been stable for ≥2 weeks before the start of treatment. Subjects with sinus arrhythmia and infrequent premature ventricular contractions are eligible at the investigator's discretion.
  9. QTcF (Fridericia) >480 ms, determined as the average from three QTcF values on the triplicate ECG obtained at screening.
  10. Current evidence of seropositive status for HIV, hepatitis B (positive for HBsAg or anti-HBsAg and anti-HBcAg antibodies) or hepatitis C (positive for anti-HCV antibody or HCV-RCV-RNA quantitation) as assessed by the applicable serology testing at screening.

    1. Serology testing is not required if seronegativity is documented in the medical history and there are no clinical signs suggestive of HIV or hepatitis infection.
    2. Subjects with positive HBV serology are eligible if quantitative PCR for plasma HBV-DNA is negative and the subject will be receiving prophylaxis for potential HBV reactivation.
    3. Subjects with positive HCV serology are eligible if quantitative PCR for plasma HCV RNA is negative.
  11. Women who are pregnant or breastfeeding.
  12. History or current evidence of hypersensitivity to any of the study drugs, or of current hypersensitivity requiring systemic steroids at doses >20 mg/day prednisone equivalent.
  13. History or current evidence of any other medical or psychiatric condition or addictive disorder, or laboratory abnormality that, in the opinion of the investigator, may increase the risks associated with study participation, or require treatments that may interfere with the conduct of the study or the interpretation of study results.

    Prior treatments

  14. Received anti-CD20 monoclonal antibody (Mab) therapy within the following periods before the start of treatment

    1. Rituximab (Rituxan®): 84 days; if a subject had received rituximab within 37 Weeks before the start of treatment, then a serum rituximab level must be negative (<500 ng/mL) at screening.
    2. Obinutuzumab (Gazyva®): 184 days
    3. Ofatumumab (Arzerra®): 88 days
  15. Received therapy for NHL (except the anti-CD20 Mab therapies listed above) within 4 weeks before the start of treatment.
  16. Any investigational drug treatment from 4 weeks or 5 half-lives of the agent before the start of treatment, whichever is longer, until the EoT Visit.
  17. Received radiotherapy to tumor lesions that would be chosen as target lesions (measurable disease) within 4 weeks before the start of treatment, unless the lesion exhibited objective progression between the radiotherapy and the screening according to the Lugano Classification for NHL.

    a. Palliative radiotherapy to non-target lesions is allowed at the investigator's discretion.

  18. Received any vaccines within 28 days of the start of treatment, or likely to require vaccines at any time from the start of treatment until 28 days after the last dose of MT-3724. Injectable flu vaccine (inactivated or recombinant) is permitted at the investigator's discretion.
  19. Received systemic immune modulators within 2 weeks before the start of treatment

    1. Systemic immune modulators include but are not limited to systemic corticosteroids at doses >20 mg/day of prednisone equivalent, cyclosporine and tacrolimus.
    2. The use of non-steroidal anti-inflammatory drugs (NSAIDs) is permitted

Location

The following cities have clinical trial sites. Please check back often as locations will be updated.

Innovative Clinical Research Institute
Whittier, California 90603
United States

Boca Raton Clinical Research
Plantation, Florida 33322
United States

Rush University
Chicago, Illinois 60612
United States

University of Maryland
Baltimore, Maryland 21201
United States

University of Texas Southwestern
Dallas, Texas 75390
United States

Enrollment

For more information on enrollment in our current clinical trials, please visit clinicaltrials.gov for location information.

About Diffuse Large B-Cell Non-Hodgkin's Lymphoma

About Diffuse Large B-Cell Non-Hodgkin's Lymphoma

Diffuse large B-cell lymphoma (DLBCL) is a type of cancer that starts in white blood cells called lymphocytes. There are two types of lymphoma: Hodgkin's and non-Hodgkin's, and the each behave, grow, and respond to treatment differently. There are several types of DLBCL, with the most common being non-Hodgkin's lymphoma.

Frequently Asked Questions

A Clinical Trial is a type of research study that examines how well a potential therapy works in humans.
The purpose of this study is to evaluate the safety and tolerability of MT-3724 in combination with Lenalidomide in subjects with relapsed or refractory B-Cell NHL.
This clinical trial has certain criteria that a person has to meet to determine if they can participate. After you have discussed the trial with your doctor, specific tests will be done to see if you qualify for this study.
Molecular Templates is sponsoring this clinical trial.
There will be a total of 64 patients enrolled in this clinical trial.
Have your physician complete the contact form.

The safety and efficacy of the investigational use of this product has not been determined. There is no guarantee that the investigational use listed will be filed with and/or approved for marketing by a regulatory agency.