Efficacy and Safety of hzVSF-v13 in Patients With COVID-19 Pneumonia

COVID-19 Clinical Trial

Official title:

Efficacy and Safety of Intravenously Administered hzVSF-v13 in Patients With COVID-19 Pneumonia: a Phase II, Proof of Concept, Multicentre, Randomized, Parallel-group, Double-blind, Placebo-controlled Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04676971
• Other study ID #: hzVSF_v13-0006
• Status: Completed
• Phase: Phase 2
• Start date: December 11, 2020
• Est. completion date: October 28, 2021

Study information

• Verified date: December 2020
• Source: ImmuneMed, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Preliminarily investigate the safety and efficacy of two doses of hzVSF-v13 + SOC vs. placebo + SOC for the treatment of COVID-19 pneumonia.

Description:

Proof of concept, multicentre, randomized, parallel-group, double-blind, placebo-controlled

Recruitment information / eligibility

• Status: Completed
• Enrollment: 115
• Est. completion date: October 28, 2021
• Est. primary completion date: August 29, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Signed written informed consent from any patient capable of giving consent, or, when the patient is incapable of doing so, by his or her legal/authorized representative. Note: In accordance with the European Medicines Agency (EMA) "Guidance on the management of clinical trials during the covid-19 (coronavirus) pandemic version 3 28/04/2020", if written consent by the trial participant is not possible (for example because of physical isolation due to COVID-19 infection), consent may be given orally by the trial participant in the presence of an impartial witness.

2. Age 18 years or older.

3. Patient is currently hospitalized.

4. Diagnosis of COVID-19 pneumonia including a positive RT-PCR test for SARS-CoV-2 of any specimen and lung involvement confirmed with chest imaging (X-ray or computed tomography [CT] scan).

5. Able to comply with the study protocol.

6. Female patients must be postmenopausal (24 months of amenorrhea), surgically sterile or must agree to use an effective method of contraception throughout the study and for up to 120 days after stopping treatment. Effective contraception includes an established hormonal therapy or intrauterine device for females, and the use of a barrier contraceptive (i.e. diaphragm or condoms) with spermicide.

Exclusion Criteria:

1. Patients with known or suspected hypersensitivity to hzVSF-v13 or to any of its excipients.

2. Active tuberculosis or suspected active bacterial, fungal, viral, or other infection (besides COVID-19).

3. Anti-rejection or immunomodulatory drugs within the past 3 months.

4. Absolute neutrophil count (ANC) < 1000/µL at screening.

5. Platelet count < 50,000/ µL at screening.

6. ALT or AST > 5 x upper limit of normal (ULN) within 24 hours at screening.

7. Serum creatinine > 2 mg/dL (> 176.8 µmol/L) or estimated creatinine clearance < 30 ml/min measured or calculated by Cockroft Gault equation.

8. Pregnancy or breastfeeding.

9. Treatment with an investigational drug within 5 half-lives or 30 days (whichever is longer) of randomization (approved/investigational COVID-19 antivirals and other off-label drugs recommended by local health authorities are permitted).

10. Patients who in the opinion of the treating physician should not participate in this program (ex: severe acute respiratory distress syndrome [ARDS], septicaemia).

Related Conditions & MeSH terms

• COVID-19
• Pneumonia

Intervention

Drug:
• hzVSF-v13
Dosage form: 100mg / 200mg of hzVSF-v13 (40 mg/mL in a 5 mL vial) Frequency: Dose at Day 1, 3, 7, D14(if necessary)
• Placebo (Normal saline solution)
Dosage form: 0.9% NaCl Solution Frequency: Dose at Day 1, 3, 7, D14(if necessary)

Locations

Country	Name	City	State
Italy	UOC Pneumologia	Bergamo
Italy	Dipartimento di Medicina Interna	Milano
Russian Federation	Federal Siberian Scientific and Clinical Center of the Federal Medical and Biological Agency	Krasnoyarsk
Russian Federation	Central City Hospital of Novoshakhtinsk	Novoshakhtinsk
Russian Federation	Pokrovskaya Municipal Hospita	Petersburg
Russian Federation	SPb SBIH "Municipal Hospital ?40"	Petersburg
Russian Federation	Regional Clinical Hospital	Saratov
Russian Federation	Regional Clinical Hospital No1	Smolensk
Russian Federation	Federal State Budgetary Educational Institution of Higher Education	Ufa

Sponsors (1)

Lead Sponsor	Collaborator
ImmuneMed, Inc.

Countries where clinical trial is conducted

Italy,  Russian Federation, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Clinical failure at Day 28	A patient will be considered a clinical failure if on Day 28 the patient is dead, intubated and/or in ICU.	Day 28
Secondary	Clinical Improvement, defined as a decrease of at least 2 points on the World Health Organization (WHO) ordinal scale	Clinical improvement is defined as a decrease of at least two points on the WHO ordinal scale from the Day 1 visit to the Day 28 visit.	Day 28
Secondary	Rate of overall survival (OS) at Day 28 and Day 60	Overall survival (OS), defined as the time from randomization to the date of death due to any cause, will be analysed by means of Kaplan-Meier methodology.	Day 28, Day 60
Secondary	Incidence and severity of adverse events according to NCI CTCAE v5.0	The incidence of AEs will be tabulated by MedDRA System Organ Class and Preferred Term. The incidence of AEs will also be summarised by System Organ Class, Preferred Term, and severity (based on NCI CTCAE v5.0 grades)	Day 60