A Study to Evaluate the Safety, Pharmacokinetics and Antiviral Effects of Galidesivir in Yellow Fever or COVID-19

NCT ID: NCT03891420

Last Updated: 2021-05-27

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1
• Total Enrollment: 24 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-04-09
• Study Completion Date: 2021-04-30

Brief Summary

This is a placebo-controlled, randomized, double-blind study to evaluate the pharmacokinetics, safety and antiviral activity of galidesivir in subjects with yellow fever (YF) or COVID-19.

Detailed Description

This is a randomized, double-blind, placebo-controlled study to evaluate the pharmacokinetics (PK), safety, and antiviral effects of galidesivir administered via intravenous (IV) infusion vs. placebo in hospitalized adult subjects with either Yellow Fever (Group A) or COVID-19 (Group B). The study will be conducted in two parts, and each Group (A or B) will proceed independently through the study. Part 1 is a dose ranging study with three sequential cohorts of eight patients each that will be randomized 3:1 to receive IV galidesivir or placebo every 12 hours for 7 days. Upon completion of part 1, an optimized dosing regimen of galidesivir will be selected for part 2, based on part 1 results including safety, PK, viral load reduction, and improvement in signs and symptoms and clinical manifestations, and mortality. In part 2, up to 42 patients will be randomized 2:1 to receive IV galidesivir or placebo. After treatment, the patients will remain hospitalized until resolution of symptoms allows release. All patients will be followed for mortality through Day 56.

Conditions

COVID-19; Yellow Fever

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Galidesivir

Galidesivir IV infusion

Group Type: EXPERIMENTAL

Galidesivir

Intervention Type: DRUG

Galidesivir IV infusion

Placebo

Placebo IV infusion

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Placebo IV infusion

Interventions

Galidesivir

Galidesivir IV infusion

Intervention Type: DRUG

Placebo

Placebo IV infusion

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Ability to provide written informed consent
• Males and nonpregnant, non-breast-feeding females, aged 18 years or older
• Subject weight ≥ 50 kg (110 lb.)
• Positive test for YFV by molecular amplification of the virus in the blood
• First onset of symptoms of YF occurring within the previous 7 days
• CLCR of at least 60 mL/min by Cockcroft-Gault equation
• AST < 5000 u/L
• Indirect bilirubin < 1.5 mg/dL
• Neutrophil count < 7500 /mm3
• International Normalized Ratio (INR) < 1.5

• Ability to provide written informed consent, accept randomization to any assigned treatment arm, and comply with planned study procedures
• Males and nonpregnant, non-breast-feeding females, aged 18 years or older
• Subject weight ≥ 50 kg (110 lb.)
• Clinical syndrome consistent with moderate-severe (but not critically ill) COVID-19, defined by at least one of the following:

1. Symptoms of acute viral lower respiratory tract infection, such as fever, non-productive cough, dyspnea, and either 1) a pulse oximetry oxygen saturation (SpO2) ≤ 94% or a respiratory rate > 24 breaths/minute as measured at rest without use of supplemental oxygen or 2) a clinical requirement for supplemental oxygen treatment or non-invasive mechanical ventilation

2. Radiographic pulmonary findings seen on chest imaging (chest X-ray or computed tomography [CT scan]) consistent with COVID-19

• Positive test for SARS-CoV-2 by molecular amplification of the virus in a respiratory specimen (nasopharyngeal, oropharyngeal, lower respiratory tract [eg, expectorated sputum]) collected < 96 hours prior to randomization. Note: subjects may have a positive test recorded prior to screening if they are admitted to the hospital with a presumed case of COVID-19

Exclusion Criteria

• Any clinically significant medical condition or medical history that, in the opinion of the investigator or sponsor, would interfere with the subject's ability to participate in the study or increase the risk of participation for that subject
• Employment by the study site, or an immediate family relationship to either study site employees or Sponsor employee
• Lack of suitable veins for venipuncture/cannulation as assessed by the Investigator at Screening
• Participation in any other investigational drug or vaccine study currently or within the past 30 days
• Diagnosis of YF vaccine-related viscerotropic disease
• Subjects with hepatic encephalopathy as defined by Conn Score ≥ 1.
• Subject has severe immunosuppression or immunodeficiency, leukemia, lymphoma, thymic disease, generalized malignancy, or radiation therapy (within the past 3 months), or is undergoing current treatment with immunosuppressive drugs, defined as drugs that impair immune responses to infections
• A treatment plan for YF that would include concomitant administration of antiviral medications

• Any clinically significant medical condition or medical history that, in the opinion of the investigator or sponsor, would interfere with the subject's ability to participate in the study or increase the risk of participation for the subject
• Lack of suitable veins for venipuncture/cannulation as assessed by the Investigator at Screening
• Participation in any other investigational drug or vaccine study currently or within the past 30 days
• A clinical treatment plan that would include concomitant administration of any other experimental treatment or off-label use of marketed medications that are intended as specific treatment for the COVID-19 clinical syndrome or the SARS-CoV-2 infection. Any such medications must be discontinued prior to study enrollment, unless a formal written standard of care policy document from the national, state, or institutional authorities requires otherwise.
• Severe or rapidly progressive disease or medical condition of any type such that death is an expected or likely outcome within 72 hours or that would require referral or transfer to another medical facility
• Severe renal impairment (estimated glomerular filtration rate (eGFR) ≤ 50 mL/min/1.73m2) or receiving continuous renal replacement therapy, hemodialysis, or peritoneal dialysis
• Severe liver disease by medical history or ALT or AST > 5 times upper limit of normal
• Congestive heart failure by medical history ≥ Class 3
• Requiring invasive mechanical ventilation or extracorporeal membrane oxygenation (ECMO) at the time of randomization

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Institute of Allergy and Infectious Diseases (NIAID)

NIH

Sponsor Role: collaborator

BioCryst Pharmaceuticals

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Esper Kallas, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Sao Paulo, Brazil

Locations

Hospital de Clinicas da Universidade Federal do Parana

Curitiba, Paraná, Brazil

Hospital Sao Vicente de Paulo-PPDS

Passo Fundo, Rio Grande do Sul, Brazil

Hospital Sao Lucas da Pucrs

Porto Alegre, Rio Grande do Sul, Brazil

Foundation Regional Faculty of Medicine of São José do Rio Preto

São José do Rio Preto, São Paulo, Brazil

Clinical Research Unit and Department of Infectious and Parasitic Diseases Hospital das Clínicas, School of Medicine, USP

São Paulo, São Paulo, Brazil

Countries

Brazil

Other Identifiers

272201300017C-18-0-1

Identifier Type: NIH

Identifier Source: secondary_id

View Link

DMID18-0022

Identifier Type: OTHER

Identifier Source: secondary_id

BCX4430-108

Identifier Type: -

Identifier Source: org_study_id