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CompletedNCT02395601Updated May 18, 2022

A Study Evaluating CPI-1205 in Patients With B-Cell Lymphomas

A Phase 1 interventional study of CPI-1205 in B-Cell Lymphoma, sponsored by Constellation Pharmaceuticals. Completed at 6 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-05-18.

Sponsored by Constellation Pharmaceuticals · Phase 1, Interventional, and Treatment

Phase
Phase 1
Study type
Interventional
Enrollment
41
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

First in human, open-label, sequential dose escalation and expansion study of CPI-1205 in patients with progressive B-cell lymphomas. CPI-1205 is a small molecule inhibitor of EZH2.

02

Conditions studied

  • B-Cell Lymphoma

Keywords

  • B-Cell Lymphoma
  • EZH2 Inhibitor
  • Phase 1
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

Adults (aged ≥ 18 years)

Histologically confirmed diagnosis of a B-cell lymphoma that has progressed in spite of prior treatment, and for which additional effective standard therapy is not available

Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2

Adequate hematological, renal, hepatic, and coagulation laboratory assessments

Must give written informed consent to participate in this study before the performance of any study-related procedure

Exclusion criteria

Exclusion Criteria:

A primary lymphoma of the central nervous system (CNS) or known lymphomatous involvement of the CNS

Impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of CPI-1205, including any unresolved nausea, vomiting, or diarrhea that is CTCAE grade >1

Treatment with proton pump inhibitors, H2 antagonists, or antacids

Achlorhydria, either documented or suspected on the basis of an associated disease (e.g., pernicious anemia, atrophic gastritis, or certain gastric surgical procedures)

Impaired cardiac function or clinically significant cardiac diseases, including any of the following:

  • Acute myocardial infarction or angina pectoris ≤ 6 months prior to starting study drug
  • New York Heart Association Class III or IV congestive heart failure
  • QTcF > 470 msec on the screening ECG

Uncontrolled cardiac arrhythmia (patients with rate-controlled atrial fibrillation are not excluded)

A past medical history of other clinically significant cardiovascular disease (e.g., uncontrolled hypertension, history of labile hypertension or history of poor compliance with an antihypertensive regimen)

Any other concurrent severe and/or uncontrolled concomitant medical condition that could compromise participation in the study (e.g., clinically significant pulmonary disease, clinically significant neurological disorder, active or uncontrolled infection)

Systemic anti-cancer treatment or radiotherapy less than 2 weeks before the first dose of CPI 1205

Radioimmunotherapy (e.g., 131I-tositumomab, 90Y-ibritumomab tiuxetan) less than 6 weeks before the first dose of CPI-1205

Treatment with an investigational small molecule less than 2 weeks before the first dose of CPI-1205.

Treatment with a therapeutic antibody less than 4 weeks before the first dose of CPI-1205.

Treatment with medications that are strong inhibitors of CYP3A4

Treatment with medications that are inducers of CYP3A4 enzymes

Treatment with medications that are known to carry a risk of Torsades de Pointes

Pregnant or lactating women

Women of child bearing potential and men with reproductive potential, if they are unwilling to use adequate contraception while on study therapy and for 3 months thereafter

Patients unwilling or unable to comply with this study protocol

04

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
41 participants (estimated)

Study arms

  • Experimental
    CPI-1205

    Drug: CPI-1205

Interventions

  • DrugCPI-1205

    Small molecule inhibitor of the enzyme EZH2

05

What researchers measure

Primary outcomes

  1. Frequency of Dose-limiting toxicities (DLTs)

    Frequency of dose-limiting toxicities (DLTs) associated with CPI-1205 administration during the first cycle (first 28 days) of treatment

    Time frame: DLTs asessed during Cycle 1 (first 28 days on study)

Secondary outcomes

  1. Frequency of adverse events

    Safety and tolerability of CPI-1205 as assessed by: frequency of adverse events and serious adverse events; changes in hematology and clinical chemistry values; changes in physical examination, vital signs, electrocardiogram, and ECOG score

    Time frame: Assessed from Day 1 of Cycle 1 through 30 days after patient's last dose of study drug

  2. Pharmacokinetic parameters of CPI-1205: AUC(0-t), AUC(0-inf), AUCtau,ss, Tmax, Cmax, Ctrough, T1/2, Vd/F, CL/F

    Time frame: Assessed during cycle 1 (first 28 days on study); and on cycle 2, day 1

  3. Pharmacodynamic effects of CPI-1205 in lymphoma tissue: changes in levels of the trimethylated form of lysine residue 27 on histone 3; changes in the expression of genes whose transcription may be altered by EZH2 inhibition

    Time frame: Assessed during cycle 1 (first 28 days on study)

  4. Pharmacodynamic effects of CPI-1205 in bone marrow and in skin: changes in global levels of the trimethylated form of lysine residue 27 on histone 3 (H3K27me3)

    Time frame: Assessed during cycle 1 (first 28 days on study)

  5. Disease response assessment will be performed using the 2014 Lugano Response Criteria for Hodgkin and Non-Hodgkin Lymphoma

    Time frame: After every 2 cycles of treatment for the first 6 cycles, and after every 4 cycles thereafter

06

Study locations

6 sites
  • Horizon Oncology Center
    Lafayette, Indiana 47905, United States
  • Massachusetts General Hospital
    Boston, Massachusetts 02114, United States
  • University of Nebraska Medical Center
    Omaha, Nebraska 68198, United States
  • John Theurer Cancer Center
    Hackensack, New Jersey 07601, United States
  • The Ohio State University James Cancer Hospital
    Columbus, Ohio 43210, United States
  • Sarah Cannon Research Institute
    Nashville, Tennessee 37203, United States
07

Registry details

Key details

Study ID
NCT02395601
Lead sponsor
Constellation Pharmaceuticals
Responsible party
Sponsor
First posted
Mar 23, 2015
Start date
Mar 2015
Primary completion
Dec 2018
Completion
Dec 2018
Last update
May 18, 2022

Oversight

Data monitoring committee
No
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