A Phase Ib Study of NVX-508 in Sickle Cell Disease

July 12, 2018 updated by: Amma Owusu-Ansah, MD

A Phase Ib, Dose-finding and Pharmacodynamic Study of NVX-508 in Sickle Cell Disease Patients

This Phase 1b study in adults with sickle cell disease (SCD) in steady-state (non-acutely ill) aims to evaluate safety and toxicity of NVX-508 in a multi-dosing paradigm as well as to determine the maximum tolerated dose (MTD) in this population. The information gained from this study will be used in making decisions about the appropriate dose(s) and dosing schedule in future multicenter studies of the efficacy of NVX-508 in the treatment of vaso-occlusive episodes (VOE).

Study Overview

Status

Withdrawn

Conditions

Intervention / Treatment

Detailed Description

Sickle cell disease (SCD) is a genetic disorder of hemoglobin that affects millions of individuals worldwide, with sub-Saharan Africa bearing the greatest burden of disease. The leading causes of hospitalization and death in individuals with sickle cell disease are painful VOE (associated with tissue injury from reduced oxygen supply) and "acute chest syndrome" respectively. Acute chest syndrome (ACS) is a form of acute lung injury unique to SCD that arises de novo or during the course of painful VOE.

A safe, reliable therapeutic deployed early in the course of painful VOE (with or without ACS) that restores oxygen supply to tissues, could potentially attenuate tissue injury, resolve pain and improve patient outcomes.

NVX-508 is a liquid fluorocarbon which transports oxygen. Stoichiometrically, NVX-508 has 200 times the oxygen carrying capacity of human hemoglobin.Oxygen is taken up by NVX-508 as it circulates through the alveolar capillary bed in the lungs and is released in blood and tissues with low oxygen content. Consequently, if it were administered intravenously (IV) and passed through the lungs of patients, it would take up oxygen, increasing the oxygen concentration in blood in a dose-dependent manner and release it to tissues with low oxygen.

The active component of NVX-508 was originally developed as an ultrasound contrast agent. It has been tested as such in over 2200 patients to whom it was safely administered as a bolus IV injection.The pharmacokinetics of NVX-508 in humans exhibits a biphasic decline after an iv bolus dose; a rapid initial decline followed by a slow terminal phase. The terminal phase t1/2 (half- life) ranges from 81-99.5 min for doses of 0.15-0.35 ml/kg. NVX-508 is not metabolized in humans, it is removed from the body unchanged in the breath (expired air) .

The rationale for studying NVX-508 for SCD is based on data from preclinical studies in the mouse model of ACS. NVX-508 when used as rescue therapy in the mouse model, restored oxygen saturation to baseline in mice experiencing hypoxemia, with 100% survival. NVX-508 reduced pulmonary vascular congestion in SCD mice experiencing ACS.

Hypothesis: Intravenous delivery of 4 doses of NVX-508 of up to 0.17 ml/kg per dose, infused over 30 minutes will be well tolerated.

Experimental design: Dose-ranging study in adults with diagnosis of SCD (SS, SC, S-Beta + thalassemia, S-Beta0 thalassemia, and SS/S-Hemoglobin D (SD)or S in combination with another variant hemoglobin) , who are in steady state (no painful episode, hospitalization or blood transfusion in the preceding 4 weeks) will be recruited from a single institution (Ghana Institute of Clinical Genetics, Korle-Bu, Accra, Ghana) to participate in the study.

The study has a 3 + 3 design. The first cohort of 3 subjects enrolled in the study shall be administered one dose (0.05 mL/kg) of NVX-508, the next cohort of 3 will be treated using two doses of NVX-508 at 0.05 mL/kg and subsequent cohort will be assigned to four doses of NVX-508. Higher doses of 0.1ml/kg and 0.17ml/kg will be administered Intra-patient dose escalation will not be allowed. Each dose shall be administered as slow IV push over 5-10 minutes with the next dose administered no less than 90 minutes after cessation of the prior infusion, but not more than 120 minutes later.

Within each cohort, when the first subject is treated, there will be a 72 hour observation interval before the next two subjects are treated at the same dose.

Study Procedures

A maximum of 24 adults with sickle cell disease aged 18 years and above will be recruited into the study.

Screening - After giving informed consent, potential study participants will undergo screening which comprises a standardized history and physical examination, lab tests (blood counts, serum chemistries) and electrocardiogram( EKG). Eligible participants will return within a week to be enrolled in the study.

Intervention - Study participants will go to a designated staffed phase I center for administration of the study drug. They will have baseline evaluations (arterial blood gas evaluation, hemoglobin and EKG) done prior to administration of the study drug. They will receive 1, 2 or 4 doses of the study drug depending They will be continuously monitored by medical research staff and the principal investigator prior to, during and in the 4 hour observation period post intervention, with physical examination, labs ( complete blood counts, serum chemistries, coagulation profile and blood samples drawn for blood gas evaluation and EKGs.

Subjects will be discharged from the clinical trials facility after the 4 hour observation period if they have had no adverse events requiring further clinical management. There will be a one week post-intervention observation period for dose-limiting toxicity for each subject, at the end of which they will have a follow up visit.

Follow up - 1 week after administration of NVX-508, subjects will have a follow-up visit at the clinical trial facility which includes history, physical exam and labs. If there are no adverse events or problems requiring continued clinical care and monitoring, subjects will exit the study once the lab and clinical data from the visit have been completely reviewed.

Study Type

Interventional

Phase

  • Phase 1

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 70 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Clinical diagnosis of SCD without acute VOE and/or ACS.
  • Age 18 years and older

  • Adequate hematologic, renal and hepatic function, defined by:

    1. Absolute neutrophil count (ANC) ≥ 1.5 x109/L
    2. Platelet count ≥ 100 x 109/L,
    3. Hemoglobin ≥ 60 g/L
    4. International normalized ratio (INR) < 1.5 x upper limit of normal (ULN)
    5. Activated partial thromboplastin time (APTT) < 1.5 x ULN
    6. Plasma creatinine < 1.5 x ULN
    7. Total bilirubin < 2.5 x ULN (in the presence of Gilbert's syndrome or indirect hyperbilirubinemia caused by hemolysis)
    8. Aspartate transaminase (AST) < 2.5 x ULN
    9. Alanine transaminase (ALT) < 2.5 x ULN
  • Ability of the prospective subject to understand and willingness to sign written informed consent document

Exclusion Criteria:

  • Patients who have received any other investigational agent within 4 weeks before enrollment.
  • Patients who have had a VOE/ACS in the previous 4 weeks before enrollment.
  • Stroke or transient ischemic attack within 6 months before enrollment.
  • Myocardial infarction within 6 months before enrollment, unstable angina, New York Heart Association class II or greater congestive heart failure, or uncontrolled hypertension (systolic BP > 160 mmHg and/or diastolic BP > 100 mmHg).
  • Congenital long QT syndrome, or corrected QT interval ( QTc) > 450 milliseconds (msec) in males and > 470 mSec in females on EKG.
  • Uncontrolled arrhythmia or any history of clinically significant arrhythmia in the past 6 months
  • Clinically-significant chronic obstructive pulmonary disease or asthma that is not controlled by medication.
  • A history of other malignancies, except adequately treated non-melanoma skin cancer, curatively treated in-situ cancer or other solid tumors curatively treated with no evidence of disease for ≥ 2 years.
  • Current anticoagulant or antiplatelet therapy, except for prophylactic doses of low molecular weight heparins or low-dose aspirin.
  • History of allergic reactions attributed to compounds of similar chemical composition to NVX- 508.
  • Women who are pregnant or breastfeeding.
  • Inability to comply with study procedures.
  • History or evidence of any other clinically-significant condition that, in the opinion of the investigator, would pose a risk to subject safety or interfere with study procedures, evaluation or completion.
  • Patients with active VOE or ACS or other significant current acute complication of SCD.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: NVX-508
Administration of 1, 2 or 4 doses of NVX-508 at three dose levels; 0.05ml/kg. 0.1ml/kg and 0.17ml/kg in a 3 + 3 design.
Drug: NVX-508
Administration of NVX-508 emulsion intravenously

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Maximum tolerated dose of NVX-508
Time Frame: 1 year
1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Amma Owusu-Ansah, MD

Collaborators

NuvOx LLC
Noguchi Memorial Institute for Medical Research

Investigators

  • Principal Investigator: Amma T Owusu-Ansah, MD, University of Pittsburgh

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

July 1, 2018

Primary Completion (Anticipated)

December 1, 2018

Study Completion (Anticipated)

December 1, 2018

Study Registration Dates

First Submitted

January 3, 2017

First Submitted That Met QC Criteria

January 4, 2017

First Posted (Estimate)

January 6, 2017

Study Record Updates

Last Update Posted (Actual)

July 16, 2018

Last Update Submitted That Met QC Criteria

July 12, 2018

Last Verified

July 1, 2018

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • PRO16110118

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

Yes

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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