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TerminatedPhase 1 / Phase 2NCT02100007
Official study title

ME-344 Given in Combination With Hycamtin® in Patients With Solid Tumors

Study summary

The purpose of this study is to determine the safety and tolerability of ME-344 when given in combination with Hycamtin® in patients with solid tumors

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Key things to know

Main goalTreatment

This describes the study’s primary purpose.

What is being studiedME-344 and Topotecan

The study team can explain what participation involves.

Who it may be forSolid Tumors

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Oct 2, 2017 · Source: ClinicalTrials.gov

Is enrollment open?Terminated

Ask the study team to confirm whether enrollment is open.

What kind of study?Phase 1 / Phase 2

Interventional

Where is it offered?10 U.S. locations

Locations may change over time.

Who runs it?MEI Pharma, Inc.

Study sponsor

01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Phase 1 / Phase 2
Sponsor
MEI Pharma, Inc.
Interventions being studied
Drug: ME-344; Drug: Topotecan
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.

Requirements people may need to meetInclusion criteria
  • Histologic or cytologic confirmed locally advanced or metastatic small cell lung cancer, ovarian cancer, or cervical cancer (Part 1); small cell lung cancer and ovarian cancer (Part 2)
  • Patients with ovarian and small cell lung cancer must have failed initial therapy
  • Patients with carcinoma of the cervix must have advanced disease not amenable to curative surgery and/or radiation therapy
  • Patients may not have received more than 4 prior regimens of therapy
  • Patients may not previously have received irinotecan, topotecan or other topoisomerase I inhibitor
  • ECOG Performance status 0-1 (Appendix B)
  • A minimum life expectancy of 12 weeks
  • Adequate bone marrow, hepatic and renal function as evidenced by:
  • Absolute neutrophil count (ANC) \> 1.5 x 109/L
  • Platelet count \> 100 x 109/L
  • Hemoglobin \> 9.0 g/dL
  • Serum bilirubin \< 1.5 x ULN
  • AST/ALT (SGOT/SGPT) \< 2.5 x ULN for the reference laboratory or \< 5 x --ULN in the presence of liver metastases
  • Serum creatinine \< 1.5 x ULN or creatinine clearance ≥ 60 mL/min as measured by institutional standards
  • At least 21 days must have elapsed prior to Day 1 Cycle 1, since any radiotherapy, immunotherapy or following major surgery; any surgical incision should be completely healed. At least 14 days must have elapsed prior to Day 1 Cycle 1 since "limited palliative radiotherapy", defined as a course of therapy encompassing \<25% total bone marrow volume and not exceeding 30 GY.
Reasons someone may not be able to joinExclusion criteria
  • Patients with tumor involvement of the Central Nervous System (CNS). SCLC patients with previously treated CNS lesions must have stable CNS disease for at least 4 weeks
  • Patients with uncontrolled infection or systemic disease
  • Patients with clinically significant cardiac disease not well controlled with medication (e.g., congestive heart failure, symptomatic coronary artery disease e.g. angina, and cardiac arrhythmias) or myocardial infarction within the last 12 months
  • Patients who have toxicity from last prior therapy that has not recovered to at least Grade 1, with the exception of Grade 2 alopecia
  • Patients who have had any chemotherapy regimens, biologic, or targeted therapies within the 2 weeks prior to Cycle 1 Day 1
  • Patients with any neuropathy \> Grade 1
  • Patients with known hypersensitivity to any components of ME-344 or topotecan study drug product
  • Patients with known human immunodeficiency virus (HIV) or Hepatitis B or C (active, previously treated or both)
  • Patients with a history of solid organ transplantation
  • Patients with presence of concurrent or active malignant disease (other than disease under study) within the last 12 months with the exception of adequately treated in-situ carcinomas, basal or squamous cell carcinoma, or non-melanomatous skin cancer. Patients with any psychiatric disorder or social or geographic situation that would preclude study participation

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Pinnacle Oncology HematologyScottsdale, Arizona
  • University of Colorado Cancer CenterAurora, Colorado
  • Northwestern UniversityChicago, Illinois
  • Oncology Hematology CareCincinnati, Ohio
  • University of OklahomaOklahoma City, Oklahoma
  • Medical University of South CarolinaCharleston, South Carolina
  • Tennessee Oncology, PLLCNashville, Tennessee
  • University of WA Seattle Cancer Care AllianceSeattle, Washington
  • The Bays St Mary's HospitalLondon, England
  • Sarah Cannon Research Instititute UKLondon, England

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Oct 2, 2017. Always confirm current availability with the study team.

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