Clinical Trial - NCT03600649

Clinical Trial of SP-2577 (Seclidemstat) in Patients With Relapsed or Refractory Ewing Sarcoma

Recruiting

Sponsor: Salarius Pharmaceuticals, LLC

Collaborators: National Pediatric Cancer Foundation

Information provided by (Responsible party): Sponsor

ClinicalTrials.gov Identifier: NCT03600649

Protocol Info

Short Description: Phase I of LSD1 Inhibitor SP-2577 in Relapsed or Refractory Ewing Sarcoma
Long Description: Phase I Trial of the LSD1 Inhibitor SP-2577 in Patients With Relapsed or Refractory Ewing Sarcoma
MGH Status: Open
Sponsor: Salarius Pharmaceuticals
Disease Program: Sarcoma

Next Steps


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Purpose

Phase 1, open-label, non-randomized dose finding study of SP-2577 in patients with refractory or recurrent Ewing sarcoma.
Condition Title Intervention Phase
Ewing Sarcoma SP-2577 Phase 1
Study Type Interventional
Official Title Phase 1 Trial of the LSD1 Inhibitor SP-2577 in Patients With Relapsed or Refractory Ewing Sarcoma

Primary Outcome Measures

Safety and tolerability of SP-2577: Assessed by the National Cancer Institute Common Terminology Criteria for Adverse Events, version 5.0 [Time Frame: From screening through at least 30 days after end of treatment, up to approximately 24 months] [Designated as safety issue: ]


Secondary Outcome Measures

Determine the maximum tolerated dose of SP-2577 [Time Frame: DLTs within the first cycle of therapy (up to 28 days)] [Designated as safety issue: ]

Characterization of the pharmacokinetics of SP-2577 [Time Frame: At protocol defined time points on cycle 1 (each cycle is 28 days), day 1 and 2 and cycle 2, day 1 and 2.] [Designated as safety issue: ]

Characterization of the pharmacokinetics of SP-2577 [Time Frame: At protocol defined time points on cycle 1 (each cycle is 28 days), day 1 and 2 and cycle 2, day 1 and 2.] [Designated as safety issue: ]

Characterization of the pharmacokinetics of SP-2577 [Time Frame: At protocol defined time points on cycle 1 (each cycle is 28 days), day 1 and 2 and cycle 2, day 1 and 2.] [Designated as safety issue: ]

Characterization of the pharmacokinetics of SP-2577 [Time Frame: At protocol defined time points on cycle 1 (each cycle is 28 days), day 1 and 2 and cycle 2, day 1 and 2.] [Designated as safety issue: ]

Characterization of the pharmacokinetics of SP-2577 [Time Frame: At protocol defined time points on cycle 1 (each cycle is 28 days), day 1 and 2 and cycle 2, day 1 and 2.] [Designated as safety issue: ]

Characterization of the pharmacokinetics of SP-2577 [Time Frame: At protocol defined time points on cycle 1 (each cycle is 28 days), day 1 and 2 and cycle 2, day 1 and 2.] [Designated as safety issue: ]

Efficacy parameter: overall response rate of SP-2577 [Time Frame: From start of treatment through at least 30 days after end of treatment, up to approximately 24 months] [Designated as safety issue: ]

Efficacy parameter: duration of response of SP-2577 [Time Frame: From start of treatment through at least 30 days after end of treatment, up to approximately 24 months] [Designated as safety issue: ]

Efficacy parameter: progression-free survival of SP-2577 [Time Frame: From start of treatment through at least 30 days after end of treatment, up to approximately 24 months] [Designated as safety issue: ]

Estimated Enrollment: 50
Study Start Date: June 2018
Estimated Study Completion Date: December 2021
Estimated Primary Completion Date: June 2020
Arms Assigned Interventions

Experimental:SP-2577

Twice-daily administration of oral SP-2577
Drug:SP-2577
Dose escalation and dose expansion of SP-2577

Eligibility

Ages Eligible for Study: N/A-N/A

Genders Eligible for Study: All

Accepts Healthly Volunteers: No

Inclusion Criteria:

  • Patients must have a histologic confirmed diagnosis of Ewing sarcoma that is refractory or recurrent and must have received at least one prior course of therapy for Ewing sarcoma. For the purposes of this study, refractory disease is defined as metastatic or unresectable disease that has either progressed or is stable at completion of planned therapy.
  • Expansion Phase Only: Patients must have measurable disease by computed tomography (CT) or magnetic resonance imaging (MRI) based on Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1. Note: Patients do not need to have measurable disease in either the accelerated or 3+3 cohorts.
  • Patients must have had prior camptothecin-based regimen, have a contraindication to camptothecin-based regimen, or declined treatment with a camptothecin-based regimen.
  • Age = 12 years and weight = 40 kg.
  • Karnofsky =70% for over =16 years old and Lansky =70% for under 16 years old, equivalent to Eastern Cooperative Oncology Group (ECOG) performance status grade 0 or 1
  • Life expectancy of greater than 4 months.
  • Patients must have normal organ and marrow function
  • Archival tumor tissue available for translocation analysis or willingness to provide tumor biopsy during screening.
  • Willingness to provide tumor biopsies during screening and while on treatment (Dose expansion cohort only). Optional for patients < 18 years of age.
  • Ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria:

  • Patients who have not recovered to grade 1 or baseline from adverse events related to prior therapy excluding lymphopenia, alopecia, peripheral neuropathy and ototoxicity, which are excluded if = CTCAE grade 3.
  • Patients who are receiving any other investigational agents.
  • Prior therapy with LSD1 targeted agents including monoamine oxidases for cancer therapy.
  • Prior systemic anti-cancer treatment (chemotherapy, biologic therapy [ie. small molecular inhibitors, monoclonal antibodies]) within 21 days prior to Cycle 1 Day 1.
  • Prior therapy with immunotherapy such as a checkpoint inhibitor, cellular therapy or vaccine therapy within 28 days prior to Cycle 1 Day 1.
  • Prior small port palliative radiotherapy within 14 days of Cycle 1 Day 1 or within 42 days of Cycle 1 Day 1 from definitive local control radiation (any dose greater than 50 Gy, within 42 days of Cycle 1 Day1).
  • Prior therapy with long acting myeloid growth factor within 14 days or 7 days from a short acting myeloid growth factor.
  • Evidence of graft versus host disease or prior allo- or auto-bone marrow transplant (BMT) or stem cell infusion within 84 days from Cycle 1 Day 1 or receiving immunosuppression following a stem cell procedure.
  • Participation in a prior investigational study within 30 days prior to Cycle 1 Day 1 or within 5-half-lives of the investigational product, whichever is longer.
  • Patients with progressive or symptomatic brain metastases. Patients with brain metastases may be included in this trial as long as the brain metastases have received definitive treatment and are stable (i.e., no evidence of progression). The brain metastases must be stable for a minimum of 6 weeks.
  • Patients currently receiving any of the following substances and cannot be discontinued 14 days or 5 half-lives for CYP inhibitors (whichever is shorter) prior to Cycle 1 Day 1: Moderate or strong inhibitors or inducers of major CYP isoenzymes, including grapefruit, grapefruit hybrids, pomelos, star fruit, and Seville oranges; Moderate or strong inhibitors or inducers of major drug transporters; Substrates of CYP3A4/5 with a narrow therapeutic index
  • Uncontrolled concurrent illness including, but not limited to: ongoing or active infection; transfusion dependent thrombocytopenia or anemia; psychiatric illness/social situations that would limit compliance with study requirements
  • Clinically significant, uncontrolled heart disease and/or cardiac repolarization abnormality, including any of the following: symptomatic congestive heart failure; Left Ventricular Ejection Fraction (LVEF) = 50%; unstable angina pectoris or cardiac arrhythmia; baseline QTc = 450 milliseconds; Long QT syndrome or family history of idiopathic sudden death or congenital long QT syndrome
  • Any major surgery within 21 days prior to Cycle 1 Day 1.
  • Pregnant and breastfeeding women
  • Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation.
  • HIV-positive patients on combination antiretroviral therapy are ineligible because of the potential for pharmacokinetic interactions with SP-2577. In addition, these patients are at increased risk of lethal infections when treated with marrow-suppressive therapy.

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT03600649

Locations

  • United States, California
    • Children's Hospital Los Angeles Los Angeles, California, United States, 90027
    • Sarcoma Oncology Research Center Santa Monica, California, United States, 90403
  • United States, Florida
    • Johns Hopkins All Children's Hospital Saint Petersburg, Florida, United States, 33701
    • H. Lee Moffitt Cancer Center and Research Institute Tampa, Florida, United States, 33612
  • United States, Massachusetts
    • Dana-Farber Cancer Institute Boston, Massachusetts, United States, 02215
  • United States, New York
    • Memorial Sloan Kettering Cancer Center New York, New York, United States, 10065
  • United States, Ohio
    • The Research Institute at Nationwide Children's Hospital Columbus, Ohio, United States, 43205
  • United States, Texas
    • MD Anderson Cancer Center Houston, Texas, United States, 77030

Sponsors and Collaborators

Salarius Pharmaceuticals, LLC

National Pediatric Cancer Foundation

More Information

No publications provided

Responsible Party: Sponsor
ClinicalTrials.gov Identifier: NCT03600649
Other Study ID Numbers:
Study First Received:
Last Updated:
Health Authority:

Additional relevant MeSH terms:

Sarcoma

Sarcoma, Ewing

Next Steps


If you are interested in this protocol or in other treatment options at Massachusetts General Hospital, please Request a Consultation.







ClinicalTrials.gov processed this data on October 14, 2020