Safety, Tolerability and Immunogenicity of INO-4800 Followed by Electroporation in Healthy Volunteers for COVID19
clinical trial
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Safety, Tolerability and Immunogenicity of INO-4800 Followed by Electroporation in Healthy Volunteers for COVID19
Summary
Safety, Tolerability and Immunogenicity of INO-4800 Followed by Electroporation in Healthy Volunteers for COVID19 is a clinical trial[1].
Key Facts
- Safety, Tolerability and Immunogenicity of INO-4800 Followed by Electroporation in Healthy Volunteers for COVID19 is in the country of South Korea[2].
- Safety, Tolerability and Immunogenicity of INO-4800 Followed by Electroporation in Healthy Volunteers for COVID19's instance of is recorded as clinical trial[3].
- Safety, Tolerability and Immunogenicity of INO-4800 Followed by Electroporation in Healthy Volunteers for COVID19's start time is recorded as +2020-06-22T00:00:00Z[4].
- Safety, Tolerability and Immunogenicity of INO-4800 Followed by Electroporation in Healthy Volunteers for COVID19's end time is recorded as +2022-02-22T00:00:00Z[5].
- Safety, Tolerability and Immunogenicity of INO-4800 Followed by Electroporation in Healthy Volunteers for COVID19's main subject is recorded as INO-4800[6].
- Safety, Tolerability and Immunogenicity of INO-4800 Followed by Electroporation in Healthy Volunteers for COVID19's main subject is recorded as severe acute respiratory syndrome[7].
- Safety, Tolerability and Immunogenicity of INO-4800 Followed by Electroporation in Healthy Volunteers for COVID19's number of participants is recorded as {'unit': '1', 'amount': '+160'}[8].
- Safety, Tolerability and Immunogenicity of INO-4800 Followed by Electroporation in Healthy Volunteers for COVID19's title is recorded as A Phase I/IIa, Dose-Ranging Trial to Evaluate Safety, Tolerability and Immunogenicity of INO-4800, a Prophylactic Vaccine Against SARS-CoV-2, Administered Intradermally Followed by Electroporation in Healthy Volunteers[9].
- Safety, Tolerability and Immunogenicity of INO-4800 Followed by Electroporation in Healthy Volunteers for COVID19's minimum age is recorded as {'unit': 'http://www.wikidata.org/entity/Q577', 'amount': '+19'}[10].
- Safety, Tolerability and Immunogenicity of INO-4800 Followed by Electroporation in Healthy Volunteers for COVID19's ClinicalTrials.gov ID is recorded as NCT04447781[11].
- Safety, Tolerability and Immunogenicity of INO-4800 Followed by Electroporation in Healthy Volunteers for COVID19's maximum age is recorded as {'unit': 'http://www.wikidata.org/entity/Q577', 'amount': '+64'}[12].
- Safety, Tolerability and Immunogenicity of INO-4800 Followed by Electroporation in Healthy Volunteers for COVID19's research intervention is recorded as citric acid[13].
- Safety, Tolerability and Immunogenicity of INO-4800 Followed by Electroporation in Healthy Volunteers for COVID19's research intervention is recorded as trisodium citrate[14].
- Safety, Tolerability and Immunogenicity of INO-4800 Followed by Electroporation in Healthy Volunteers for COVID19's research intervention is recorded as INO-4800[15].
- Safety, Tolerability and Immunogenicity of INO-4800 Followed by Electroporation in Healthy Volunteers for COVID19's clinical trial phase is recorded as phase I clinical trial[16].
- Safety, Tolerability and Immunogenicity of INO-4800 Followed by Electroporation in Healthy Volunteers for COVID19's clinical trial phase is recorded as phase II clinical trial[17].
- Safety, Tolerability and Immunogenicity of INO-4800 Followed by Electroporation in Healthy Volunteers for COVID19's research subject recruitment status is recorded as not yet recruiting[18].
- Safety, Tolerability and Immunogenicity of INO-4800 Followed by Electroporation in Healthy Volunteers for COVID19's study type is recorded as interventional study[19].