Safety, Tolerability and Immunogenicity of INO-4800 for COVID19 in Healthy Volunteers

NCT ID: NCT05430958

Last Updated: 2022-11-17

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: PHASE1
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-10-31
• Study Completion Date: 2024-03-31

Brief Summary

This is an open label, phase 1 clinical trial of an intra-dermal booster dose of INO-4800 alone or in combination with INO-9112 followed by electroporation (EP) among healthy adults at least 18 years of age, who previously completed their primary immunization series with mRNA vaccines against SARS-CoV-2 within 6-12 months prior to the booster dose.

Conditions

Coronavirus Infection

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

Group 1

Single injection of 0.8 mg of INO-4800 followed by EP administered at Day 0

Group Type: EXPERIMENTAL

INO-4800

Intervention Type: DRUG

INO-4800 will be given at 0.8 or 1.6 mg for at least 6 months but no more than 12 months following the completion of a primary vaccination.

CELLECTRA® 2000

Intervention Type: DEVICE

Electroporation (EP) using the CELLECTRA® 2000 device will be administered following ID delivery of INO-4800.

Group 2

Single injection of 0.8 mg of INO-4800 plus 0.05 mg of INO-9112 followed by EP administered at Day 0

Group Type: EXPERIMENTAL

INO-4800

Intervention Type: DRUG

INO-4800 will be given at 0.8 or 1.6 mg for at least 6 months but no more than 12 months following the completion of a primary vaccination.

INO-9112

Intervention Type: DRUG

INO-9112 will be given in at various doses (dose of 0, 0.05, 0.10, 0.20 or 0.40 mg) in combination with INO-4800.

CELLECTRA® 2000

Intervention Type: DEVICE

Electroporation (EP) using the CELLECTRA® 2000 device will be administered following ID delivery of INO-4800.

Group 3

Single injection of 0.8 mg of INO-4800 plus 0.10 mg of INO-9112 followed by EP administered at Day 0

Group Type: EXPERIMENTAL

INO-4800

Intervention Type: DRUG

INO-4800 will be given at 0.8 or 1.6 mg for at least 6 months but no more than 12 months following the completion of a primary vaccination.

INO-9112

Intervention Type: DRUG

INO-9112 will be given in at various doses (dose of 0, 0.05, 0.10, 0.20 or 0.40 mg) in combination with INO-4800.

CELLECTRA® 2000

Intervention Type: DEVICE

Electroporation (EP) using the CELLECTRA® 2000 device will be administered following ID delivery of INO-4800.

Group 4

Single injection of 0.8 mg of INO-4800 plus 0.20 mg of INO-9112 followed by EP administered at Day 0

Group Type: EXPERIMENTAL

INO-4800

Intervention Type: DRUG

INO-4800 will be given at 0.8 or 1.6 mg for at least 6 months but no more than 12 months following the completion of a primary vaccination.

INO-9112

Intervention Type: DRUG

INO-9112 will be given in at various doses (dose of 0, 0.05, 0.10, 0.20 or 0.40 mg) in combination with INO-4800.

CELLECTRA® 2000

Intervention Type: DEVICE

Electroporation (EP) using the CELLECTRA® 2000 device will be administered following ID delivery of INO-4800.

Group 5

Two injections of 0.8 mg (1.6 mg total) of INO-4800 followed by EP administered at Day 0

Group Type: EXPERIMENTAL

INO-4800

Intervention Type: DRUG

INO-4800 will be given at 0.8 or 1.6 mg for at least 6 months but no more than 12 months following the completion of a primary vaccination.

CELLECTRA® 2000

Intervention Type: DEVICE

Electroporation (EP) using the CELLECTRA® 2000 device will be administered following ID delivery of INO-4800.

Group 6

Two injections of 0.8 mg (1.6 mg total) of INO-4800 + 0.05 mg (0.1 mg total) of INO-9112 followed by EP administered at Day 0

Group Type: EXPERIMENTAL

INO-4800

Intervention Type: DRUG

INO-4800 will be given at 0.8 or 1.6 mg for at least 6 months but no more than 12 months following the completion of a primary vaccination.

INO-9112

Intervention Type: DRUG

INO-9112 will be given in at various doses (dose of 0, 0.05, 0.10, 0.20 or 0.40 mg) in combination with INO-4800.

CELLECTRA® 2000

Intervention Type: DEVICE

Electroporation (EP) using the CELLECTRA® 2000 device will be administered following ID delivery of INO-4800.

Group 7

Two injections of 0.8 mg (1.6 mg total) of INO-4800 + 0.1 mg (0.20 mg total) of INO-9112 followed by EP administered at Day 0

Group Type: EXPERIMENTAL

INO-4800

Intervention Type: DRUG

INO-4800 will be given at 0.8 or 1.6 mg for at least 6 months but no more than 12 months following the completion of a primary vaccination.

INO-9112

Intervention Type: DRUG

INO-9112 will be given in at various doses (dose of 0, 0.05, 0.10, 0.20 or 0.40 mg) in combination with INO-4800.

CELLECTRA® 2000

Intervention Type: DEVICE

Electroporation (EP) using the CELLECTRA® 2000 device will be administered following ID delivery of INO-4800.

Group 8

Two injections of 0.8 mg (1.6 mg total) of INO-4800 + 0.20 mg (0.40 mg total) of INO-9112 followed by EP administered at Day 0

Group Type: EXPERIMENTAL

INO-4800

Intervention Type: DRUG

INO-4800 will be given at 0.8 or 1.6 mg for at least 6 months but no more than 12 months following the completion of a primary vaccination.

INO-9112

Intervention Type: DRUG

INO-9112 will be given in at various doses (dose of 0, 0.05, 0.10, 0.20 or 0.40 mg) in combination with INO-4800.

CELLECTRA® 2000

Intervention Type: DEVICE

Electroporation (EP) using the CELLECTRA® 2000 device will be administered following ID delivery of INO-4800.

Interventions

INO-4800

INO-4800 will be given at 0.8 or 1.6 mg for at least 6 months but no more than 12 months following the completion of a primary vaccination.

Intervention Type: DRUG

INO-9112

INO-9112 will be given in at various doses (dose of 0, 0.05, 0.10, 0.20 or 0.40 mg) in combination with INO-4800.

Intervention Type: DRUG

CELLECTRA® 2000

Electroporation (EP) using the CELLECTRA® 2000 device will be administered following ID delivery of INO-4800.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Healthy men and non-pregnant women at least 18 years of age;
• Able and willing to comply with all study procedures;
• Screening laboratory results within normal limits or deemed not clinically significant by the Investigator;
• Received full primary series doses of an approved or authorized mRNA vaccine at least 6 months but no more than 12 months prior to INO-4800 booster dose.
• Must meet one of the following criteria with respect to reproductive capacity:

• Women who are post-menopausal as defined by reported spontaneous amenorrhea for ≥ 12 months;
• Surgically sterile (i.e., vasectomy in males or tubal ligation, absence of ovaries and/or uterus in females). In the case of vasectomy, participants should wait six (6) months post-vasectomy prior to enrollment;
• Use of medically effective contraception with a failure rate of < 1% per year when used consistently and correctly from screening until Day 28 post booster dose.

Exclusion Criteria

• Acute febrile illness with temperature >100.4°F (38.0°C) or acute onset of upper or lower respiratory tract symptoms (e.g., cough, shortness of breath, sore throat) within the prior 72 hours;
• Positive SARs-CoV-2 PCR test, if results are available prior to dosing;
• Pregnant or breastfeeding, or intending to become pregnant or intending to father children within the projected duration of the study starting from the Screening visit until Day 28 post booster dose;
• Positive pregnancy test during screening or immediately prior to booster dose;
• Positive HIV rapid test, Hepatitis B surface antigen (HBsAg) or Hepatitis C antibody at Screening;
• Is currently participating or has participated in a study with an IP within 30 days preceding Day 0 (documented receipt of placebo in a previous study would be permissible for study eligibility);
• Currently participating in another study with an investigational product during the conduct of this study;
• Previous or planned receipt of any COVID-19 booster vaccine during the trial period
• Medical conditions as follows:

• Respiratory diseases
• History of hypersensitivity or severe allergic reaction
• Uncontrolled hypertension
• Uncontrolled diabetes mellitus
• Malignancy within the past 2 years, with the exception of superficial skin
• History of cardiovascular disease
• History of myocarditis or pericarditis
• History of seizures within the past 2 years
• Underlying immunosuppressive illness
• Lack of acceptable sites for ID injection and EP
• Blood donation or transfusion within 1 month prior to Day 0;
• Reported alcohol or substance abuse/dependence or illicit drug use within the past year;
• Any non-study vaccine (e.g., influenza vaccine) within 2 weeks prior to the dose of IP.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Inovio Pharmaceuticals

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jose Suaya, MD

Role: STUDY_DIRECTOR

Inovio Pharmaceuticals

Other Identifiers

COVID19-131

Identifier Type: -

Identifier Source: org_study_id