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A Phase 2a Study of IV BCV in Subjects With Adenovirus Infection

Phase 2
Recruiting
Conditions
Adenovirus Infections
Cytomegalovirus Infection
Interventions
Drug: BCV
Registration Number
NCT04706923
Lead Sponsor
SymBio Pharmaceuticals
Brief Summary

The purpose of this study is to determine the safety and tolerability of intravenous (IV) brincidofovir (BCV; SyB V-1901) 0.2 mg/kg, 0.3 mg/kg or 0.4 mg/kg dosed twice weekly (BIW) or 0.4 mg/kg dosed once weekly (QW) for 4 weeks in subjects with AdV, and IV BCV in subjects with CMV

Detailed Description

This is a Phase IIa, open-label, multiple ascending dose confirmation, multicenter study to evaluate the safety and tolerability of intravenous Brincidofovir (BCV, SyB V-1901) 0.2 mg/kg, 0.3 mg/kg, or 0.4 mg/kg dosed BIW or 0.4 mg/kg dosed QW (Cohorts 1 to 4) in adult and pediatric subjects with AdV viremia, and IV BCV in subjects with CMV.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
52
Inclusion Criteria
  • Male or female, aged 2 months and older at the time of informed consent.
  • AdV DNA viremia >10,000 copies/mL from a single sample, or 2 samples greater than 48 hours apart with the second result higher than the first and both greater than 1000 copies/mL, from the data obtained from the designated central virology laboratory of the local laboratory using the blood sample(s) collected informed consent has been obtained and within 7 days prior to Day 1 (AdV DNA viremia results collected within the 7 day window, but prior to consent may be used if the Informed Consent Form (ICF) signed by the subject provides approval) . CMV viremia with or without evidence of tissue invasive CMV disease. For laboratory results that are generated in units other than copies/mL or IU/mL, please refer to the testing laboratory for guidance on the appropriate conversion calculation.
  • Either (a) have disseminated AdV disease or (b) have an underlying immunocompromised state, and have asymptomatic AdV infection or localized AdV disease.
  • In the judgment of the investigator, be in a serious condition to be treated with intravenous cidofovir for AdV.
Exclusion Criteria
  • Subjects who weigh ≥120 kg.
  • NIH/NCI CTCAE (United States [US] National Institutes of Health [NIH]/National Cancer Institute) Grade 2 or higher diarrhea (i.e., increase of ≥ 4 stools per day over usual pre-transplant stool output) within 7 days prior to Day 1.
  • NIH Stage 4 acute GVHD of the skin (i.e., generalized erythroderma with bullous formation) within 7 days prior to Day 1.
  • NIH Stage 2 or higher acute GVHD of the liver function (i.e., bilirubin >3 mg/dL [SI: >51 μmol/L]) within 7 days prior to Day 1.
  • NIH Stage 2 or higher acute GVHD of the gut (i.e., diarrhea >556 mL/m2/day for pediatric subjects [or >1000 mL/day for young adults as applicable, at centers in the United States only], or severe abdominal pain with or without ileus) within 7 days prior to Day 1.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
BCV 0.4 mg/kg QWBCVBCV: 0.4 mg/kg administered as a continuous IV infusion over 2 hours
BCV 0.2mg/kg BIWBCVBCV: 0.2 mg/kg administered as a continuous IV infusion over 2 hours
BCV 0.3mg/kg BIWBCVBCV: 0.3 mg/kg administered as a continuous IV infusion over 2 hours
BCV 0.4 mg/kg BIWBCVBCV: 0.4 mg/kg administered as a continuous IV infusion over 2 hours
Primary Outcome Measures
NameTimeMethod
Safety will be evaluated based on incidence and severity of Adverse Events, Serious Adverse Events and laboratory assessments.From initiation of BCV administration up to 19 weeks

Safety will be evaluated based on incidence and severity of Adverse Events, Serious Adverse Events and laboratory assessments.

Antiviral EffectsFrom initiation of BCV administration up to 9 weeks

Change from baseline AdV viremia in plasma measured on Day 1 and weekly throughout the study.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (5)

University of Nebraska Medical Center

🇺🇸

Omaha, Nebraska, United States

MD Anderson Cancer Center

🇺🇸

Houston, Texas, United States

St. Jude Children's Research Hospital

🇺🇸

Memphis, Tennessee, United States

Research Site

🇺🇸

Seattle, Washington, United States

Cincinnati Children's Hospital Medical Center

🇺🇸

Cincinnati, Ohio, United States

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