A Phase I/II Study of OPN-305 in Second-line Lower Risk Myelodysplastic Syndrome

Completed · Phase 1/Phase 2

Conditions studied: Myelodysplastic Syndrome

In brief

The dose-confirming part of this study, comprising at least 10 patients is designed as a single center, prospective, single arm, open label in patients who have failed or are unresponsive to Azacitidine (AZA) or Decitabine (they may also have additionally failed an Erythropoiesis Stimulating Agent (ESA) followed by a dose expansion part with at least 44 patients; the objective of the whole study being to assess the safety, efficacy, pharmacokinetics and pharmacodynamics of intravenously infused multiple doses of OPN-305 in low and intermediate-1 risk myelodysplastic syndrome (second and third line Lower risk MDS).

Key facts

Study ID

NCT02363491

Run by

Opsona Therapeutics Ltd.

People needed

96

Starts

2015-01-01

Expected to finish

2018-12-01

Last updated by the study team

2019-01-28

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Written informed consent
• Age ≥ 18 years
• Diagnosis of MDS (de novo or secondary) by bone marrow aspirate based on the World Health Organization (WHO) classification - Low and Intermediate-1 risk categories MDS using the IPSS (International Prognostic Scoring System)
• AZA/decitabine (this applies to standard of care and investigational drugs) failure (Dose confirming and Dose expansion parts):
• defined as discontinuation due to any of the following:
• Lack of response after at least 4 cycles
• Loss of response (patient must have received therapy for at least 4 cycles)
• Progressive disease
• Adverse events
• Note: Patients are eligible if additionally they have failed an ESA
• HMA Naïve group:
• Never received a hypomethylating agent for MDS
• Failed or ceased to respond to ESA(s)
• ESA ineligible; defined as endogenous serum erythropoietin level > 200 U/L for subjects not previously treated with ESAs
• Red blood cell transfusion dependent defined as ≥ 2 Red blood cells (RBC) units required in the 8 weeks prior to starting in the study. In addition, there should be no 8 consecutive weeks without red blood cell transfusions in the 16 weeks prior to enrolment.
• Life expectancy ≥ 3 months
• Eastern Cooperative Oncology Group (ECOG) performance status Grade 0-2
• Serum bilirubin levels ≤2 x upper limits of normal (ULN)
• Serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels ≤2.5 x ULN
• Del 5q patients who have failed or are not eligible for Revlimid
• Creatinine clearance >30 ml/min calculated by the Cockcroft-Gault formula
• Willingness to comply with the protocol procedures for the duration of the study, including scheduled follow-up visits and examinations
• Negative urine β-human chorionic gonadotropin (β-HCG) pregnancy test for fertile women at screening and confirmed by serum pregnancy test in the 48 hours prior to OPN-305 administration
• If sexually active female, patient must be/have one of the following:
• Post-menopausal defined as the absence of menses for at least one year (serum Follicle-stimulating hormone (FSH) ≥20IU/L can also be measured according to local practice),OR

You may not qualify if…

• Diagnosis of MDS by bone marrow aspirate of Intermediate-2 and High risk category MDS based on the World Health Organization (WHO) classification using the IPSS (International Prognostic Scoring System)
• Patients with 5q deletion (del) MDS eligible for Revlimid (lenalidomide)
• Hypomethylating agent (HMA) Naïve group:
• Have received a hypomethylating agent for MDS
• Have not failed or ceased to respond to an ESA
• Are not ESA ineligible as defined in inclusion criteria
• Prior history of acute leukemia or AML
• Unable/unwilling to undergo bone marrow sampling
• Prior history of bone marrow transplantation
• Prior malignancy (other than non-invasive malignancy including in situ cervical cancer, Bowen's disease, basal cell cancer of the skin and non-invasive or excised skin squamous cell carcinoma) unless treated with curative intent and without evidence of disease for 3 years before randomization
• Active viral or bacterial infections: this includes any infections that are being actively treated even if the signs and symptoms appear to have resolved. Courses of antibiotics or anti-viral treatment should be completed before the patients is enrolled
• Unstable angina, congestive heart failure [NYHA (New York Heart Association) >class II], uncontrolled hypertension [diastolic > 100 mmHg], uncontrolled cardiac arrhythmia, or recent (within 1 year) myocardial infarction, uncontrolled diabetes mellitus
• Clinical Evidence of Central Nervous System (CNS) disease
• Less than 4 weeks since any therapy for MDS
• Prior history of anaphylaxis to similar products
• History or presence of a medical condition or disease or substance abuse that in the investigator's assessment would place the patient at an unacceptable risk for study participation
• Lactating or pregnant woman

Where it is running

• Research Site — Tampa, Florida, United States
• Research Site — New York, New York, United States
• Research Site — The Bronx, New York, United States
• Research Site — Houston, Texas, United States

Full record on ClinicalTrials.gov

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