Approval Probability
TA Base Rate
Adjusted LOA
ML Risk
Also known as CoV2 preS dTM-AF03 (low-dose)
CoV2 preS dTM-AF03 · 1 trial · 1 indication
GMTs of SARS-CoV-2 neutralizing antibodies was measured using a neutralization assay. Titers were expressed in terms of 1/dilution.
GMTs of SARS-CoV-2 neutralizing antibodies was measured using a neutralization assay. Titers were expressed in terms of 1/dilution.
GMTs of SARS-CoV-2 neutralizing antibodies was measured using a neutralization assay. Titers were expressed in terms of 1/dilution.
SARS-CoV-2 neutralizing antibodies was measured using a neutralization assay. Fold-rise was calculated as the ratio of titer values of neutralizing antibodies post-vaccination (Day 22) and pre-vaccination (on Day 1) i.e., Day 22/Day 1.
SARS-CoV-2 neutralizing antibodies was measured using a neutralization assay. Fold-rise was calculated as the ratio of titer values of neutralizing antibodies post-vaccination (Day 36) and pre-vaccination (on Day 1) i.e., Day 36/Day 1.
SARS-CoV-2 neutralizing antibodies was measured using a neutralization assay. The fold rise (2-fold and 4-fold) was calculated as the ratio of titer values of neutralizing antibodies post-vaccination (on Day 22) and pre-vaccination (on Day 1) i.e., Day 22/Day 1.
SARS-CoV-2 neutralizing antibodies was measured using a neutralization assay. The fold rise (2-fold and 4-fold) was calculated as the ratio of titer values of neutralizing antibodies post-vaccination (on Day 36) and pre-vaccination (on Day 1) i.e., Day 36/Day 1.
Seroconversion was defined as participants with a Baseline (Day 1) titer value below lower limit of quantification (LLOQ) with a detectable neutralization antibody titer above assay LLOQ post vaccination (at Day 22). LLOQ of the neutralization assay was a titer of 10.
Seroconversion was defined as participants with a Baseline (Day 1) titer value below LLOQ with a detectable neutralization antibody titer above assay LLOQ post vaccination (at Day 36). LLOQ of the neutralization assay was a titer of 10.
An AE was defined as any untoward medical occurrence in a participant who received study vaccine and does not necessary had to have a causal relationship with treatment. An unsolicited AE was an observed AE that did not fulfill the conditions of solicited reactions prelisted in the case report form (CRF) in terms of diagnosis and/or onset window post-vaccination. All participants were observed for 30 minutes after vaccination, and any unsolicited systemic AEs occurred during that time were recorded as immediate unsolicited AEs in the CRF. Reported AEs for each arm were presented as pre-specified in the study protocol.
A solicited reaction (SR) was defined as an "expected" adverse reaction (AR) (sign or symptom) observed and reported under the conditions (nature and onset) prelisted (i.e., solicited) in the protocol and CRF and considered as related to vaccination. Solicited injection site reactions included pain, erythema and swelling. Reported AEs for each arm were presented as pre-specified in the study protocol.
An SR was defined as an "expected" AR (sign or symptom) observed and reported under the conditions (nature and onset) prelisted (i.e., solicited) in the protocol and CRF and considered as related to vaccination. Solicited systemic reactions included fever, headache, malaise and myalgia. Reported AEs for each arm were presented as pre-specified in the study protocol.
An AE was defined as any untoward medical occurrence in a participant who received study vaccine and does not necessary had to have a causal relationship with treatment. An unsolicited AE was an observed AE that did not fulfill the conditions of solicited reactions prelisted in the CRF in terms of diagnosis and/or onset post-vaccination. Reported AEs for each arm were presented as pre-specified in the study protocol.
A MAAE were AEs with a new onset or a worsening of a condition that prompted the participant to seek unplanned medical advice at a physician's office (including phone contact or email) or emergency department. An AE was defined as any untoward medical occurrence in a participant who received study vaccine and does not necessarily had to have a causal relationship with treatment. Reported AEs for each arm were presented as pre-specified in the study protocol.
An SAE was any untoward medical occurrence that at any dose resulted in death, was life-threatening, required inpatient hospitalization or prolongation of existing hospitalization, resulted in persistent or significant disability/incapacity, was a congenital anomaly/birth defect, or was an important medical event. Reported AEs for each arm were presented as pre-specified in the study protocol.
An AESI (serious or non-serious) was defined as one of scientific and medical concern specific to the Sponsor's product or program, for which ongoing monitoring and rapid communication by the Investigator to the Sponsor was appropriate. Reported AEs for each arm were presented as pre-specified in the study protocol.
Laboratory tests included hemoglobin (male and female), above and below normal white blood cell, lymphocytes, neutrophils \& eosinophils, platelet count, creatinine and blood urea nitrogen, hyponatremia \& hypernatremia, hyperkalemia \& hypokalemia, hyperglycemia (non-fasting), hypoproteinemia, alkaline phosphate, alanine aminotransferase, aspartate aminotransferase, bilirubin (with any increase in liver function test \[LFT\], bilirubin (normal in LFT), amylase \& lipase, Urine: protein, glucose \& blood. The US FDA Guidance for Industry "Toxicity Grading Scale for Healthy Adults and Adolescent Volunteers Enrolled in Preventive Vaccine Clinical Trials" was used for grading. As per the guidance, Grade 1 = mild, Grade 2 = moderate and Grade 3 = severe.
| Arm | Type | Description |
|---|---|---|
| Cohort 1: Group 1: SARS-CoV-2 vaccine LD + AF03 | EXPERIMENTAL | Participants received a single intramuscular (IM) injection of SARS-CoV2 vaccine low-dose (LD) formulation along with adjuvant AF03 on Day 1. |
| Cohort 1: Group 2: SARS-CoV-2 vaccine LD + AS03 | EXPERIMENTAL | Participants received a single IM injection of SARS-CoV2 vaccine LD formulation along with adjuvant AS03 on Day 1. |
| Cohort 1: Group 3: SARS-CoV-2 vaccine HD + AF03 | EXPERIMENTAL | Participants received a single IM injection of SARS-CoV2 vaccine high-dose (HD) formulation along with adjuvant AF03 on Day 1. |
| Cohort 1: Group 4: SARS-CoV-2 vaccine HD + AS03 | EXPERIMENTAL | Participants received a single IM injection of SARS-CoV2 vaccine HD formulation along with adjuvant AS03 on Day 1. |
| Cohort 1: Group 5: Placebo | PLACEBO_COMPARATOR | Participants received an IM injection of placebo matching to SARS-CoV2 vaccine on Day 1. |
| Cohort 2: Group 6: SARS-CoV-2 vaccine LD + AF03 | EXPERIMENTAL | Participants received IM injection of SARS-CoV2 vaccine LD formulation along with adjuvant AF03 on Day 1 and Day 22, respectively. |
| Cohort 2: Group 7: SARS-CoV-2 vaccine LD + AS03 | EXPERIMENTAL | Participants received IM injection of SARS-CoV2 vaccine LD formulation along with adjuvant AS03 on Day 1 and Day 22, respectively. |
| Cohort 2: Group 8: SARS-CoV-2 vaccine HD + AF03 | EXPERIMENTAL | Participants received IM injection of SARS-CoV2 vaccine HD formulation along with adjuvant AF03 on Day 1 and Day 22, respectively. |
| Cohort 2: Group 9: SARS-CoV-2 vaccine HD + AS03 | EXPERIMENTAL | Participants received IM injection of SARS-CoV2 vaccine HD formulation along with adjuvant AS03 on Day 1 and Day 22, respectively. |
| Cohort 2: Group 10: SARS-CoV-2 vaccine HD | EXPERIMENTAL | Participants received a single IM injection of SARS-CoV2 vaccine HD formulation without adjuvant on Day 1 and Day 22, respectively. |
| Cohort 2: Group 11: Placebo | PLACEBO_COMPARATOR | Participants received an IM injection of placebo matching to SARS-CoV2 on Day 1 and Day 22, respectively. |
| Name | Type | Description |
|---|---|---|
| CoV2 preS dTM-AF03 (low-dose) | BIOLOGICAL | Pharmaceutical form: liquid; route of administration: intramuscular injection |
| CoV2 preS dTM-AF03 (high-dose) | BIOLOGICAL | Pharmaceutical form: liquid; route of administration: intramuscular injection |
| CoV2 preS dTM-AS03 (low-dose) | BIOLOGICAL | Pharmaceutical form: liquid; route of administration: intramuscular injection |
| CoV2 preS dTM-AS03 (high-dose) | BIOLOGICAL | Pharmaceutical form: liquid; route of administration: intramuscular injection |
| CoV2 preS dTM (high-dose) without adjuvant | BIOLOGICAL | Pharmaceutical form: liquid; route of administration: intramuscular injection |
| Placebo (0.9% normal saline) | BIOLOGICAL | Pharmaceutical form: liquid; route of administration: intramuscular injection |
Inclusion Criteria: * Aged 18 years of age or older on the day of inclusion. * Informed consent form had been signed and dated. * Able to attend all scheduled visits and complied with all study procedures. Exclusion Criteria: * Participant was pregnant, or lactating, or of childbearing potential ...
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CoV2 preS dTM-AF03 is an investigational COVID-19 vaccine candidate developed by Sanofi. It is a recombinant protein vaccine formulation designed to prevent COVID-19 in healthy adults. The low-dose version is identified as CoV2 preS dTM-AF03 (low-dose). It has been studied in a single Phase 1 clinical trial.
CoV2 preS dTM-AF03 is being developed for the prevention of COVID-19. It was tested in healthy adult volunteers 18 years of age and older. The candidate is intended for immunization against SARS-CoV-2, the virus that causes COVID-19.
CoV2 preS dTM-AF03 is developed by Sanofi, which trades under the ticker SNY. Sanofi is the sponsor of the clinical program evaluating this recombinant protein vaccine candidate for COVID-19 prevention.
CoV2 preS dTM-AF03 is in Phase 1 clinical development. It is an investigational vaccine candidate and has not been approved by the FDA. The Phase 1 trial has been completed, and no active trials are currently listed for this candidate.
CoV2 preS dTM-AF03 was evaluated in clinical trial NCT04537208, titled Study of Recombinant Protein Vaccine Formulations Against COVID-19 in Healthy Adults 18 Years of Age and Older. The Phase 1 trial enrolled 441 participants in the United States, was randomized, double-blind, and placebo-controlled, and has been completed.
Yes. CoV2 preS dTM-AF03 (low-dose) is an alternative name for CoV2 preS dTM-AF03. The parenthetical low-dose label distinguishes the lower-dose formulation of the same Sanofi recombinant protein vaccine candidate studied in the Phase 1 COVID-19 trial.