> Trialight public data. Index of pages: https://trialight.com/llms.txt
> Web page: https://trialight.com/data/asset/rabies-vaccine-dd2dbfaf-fbe2-4e15-ad6e-b6f4041aa1c9
> Record changed: 2026-10-13

# Rabies vaccine

Highest phase reached

Phase 3

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL2107909)

Drug type

Vaccine component

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL2107909)

## Development status

**Listing at source**

Listed

**Highest phase reached**

Phase 3

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL2107909)

## Names and chemistry

**Drug type**

Vaccine component

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL2107909)

**Drug name**

Rabies vaccine

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL2107909)

### Other names (10)

- rabies vaccine
- Rabies vaccine
- Rabies Vaccine
- Rabies Vaccine (Imovax)
- Rabies vaccine (RabAvert)
- Rabies Vaccine (RabAvert)
- rabies vaccine adsorbed
- Rabies vaccine adsorbed
- rabies vaccines
- Rabies vaccines

## Identifiers

**ChEMBL ID**

CHEMBL2107909

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL2107909)

## Regulatory information

### Other regulatory facts

**First in class**

No

**Orphan designation**

No

## Pharmacology

### Investigated indications (5)

- **Condition**  
Infections

**Highest recorded phase**  
3

**Condition identifier**  
EFO:0000544

**Subject identifier**  
D007239
- **Condition**  
HIV Infections

**Highest recorded phase**  
2

**Condition identifier**  
EFO:0000764

**Subject identifier**  
D015658
- **Condition**  
Malaria

**Highest recorded phase**  
3

**Condition identifier**  
EFO:0001068

**Subject identifier**  
D008288
- **Condition**  
Malaria, Falciparum

**Highest recorded phase**  
2

**Condition identifier**  
EFO:0007444

**Subject identifier**  
D016778
- **Condition**  
Rhabdoviridae Infections

**Highest recorded phase**  
3

**Condition identifier**  
EFO:0007469

**Subject identifier**  
D018353

### Open Targets indications (6)

- **Condition identifier**  
EFO\_0000544

**Highest recorded phase**  
3
- **Condition identifier**  
EFO\_0000764

**Highest recorded phase**  
2
- **Condition identifier**  
EFO\_0001068

**Highest recorded phase**  
3
- **Condition identifier**  
EFO\_0007444

**Highest recorded phase**  
2
- **Condition identifier**  
EFO\_0007469

**Highest recorded phase**  
3
- **Condition identifier**  
MONDO\_0024618

**Highest recorded phase**  
4

### Reported adverse events (3)

- **Event**  
immune thrombocytopenic purpura

**Reports**  
9

**Reporting signal score**

52.1875
- **Event**  
laryngeal oedema

**Reports**  
3

**Reporting signal score**

12.5133
- **Event**  
urticaria

**Reports**  
5

**Reporting signal score**

9.10519

### Trial references (41)

- NCT00031070  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00031070)
- NCT00308061  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00308061)
- NCT00380393  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00380393)
- NCT00703066  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00703066)
- NCT00866619  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00866619)
- NCT01148459  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT01148459)
- NCT01635647  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT01635647)
- NCT01658696  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT01658696)
- NCT01666925  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT01666925)
- NCT03276962  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT03276962)
- NCT00317473  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00317473)
- NCT00349713  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00349713)
- NCT00358332  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00358332)
- NCT00460525  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00460525)
- NCT03435874  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT03435874)
- NCT03896724  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT03896724)
- NCT04661579  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT04661579)
- NCT05135273  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05135273)
- NCT05776017  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05776017)
- NCT05790889  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT05790889)
- NCT00703521  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00703521)
- NCT00948272  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00948272)
- NCT01228383  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT01228383)
- NCT01339312  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT01339312)
- NCT01388985  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT01388985)

And 16 more, listed on the interactive page.

## Chemical properties

**Prodrug**

No

**Chirality**

Single enantiomer

**Inorganic**

No

**Natural product**

No

## Related records

### Trials (102)

- A Bridging Study of the SYN023 on Healthy Adult Subjects
- A Clinical Trial of Rabies Vaccine（Human Diploid Cell）for Human Use,Freeze-dried in a Population Aged 10 to 60 Years
- A Clinical Trial of Rabies Vaccine（Human Diploid Cell）for Human Use,Freeze-dried in a Population Aged 10-60 Years
- A Comparison of the Safety, PD and PK of a Single Dose of SYN023 Administered With Licensed Rabies Vaccines
- A Phase 1/2b Study of an Investigational Malaria Vaccination Strategy in 5-17 Month Old Infants and Children in Burkina Faso
- A Phase 3 Clinical Trial to Evaluate Long-term Immunogenicity and Boostability of Purified Chick-Embryo Cell Rabies Vaccine in Adults Following Primary Series of Pre/Exposure Prophylaxis.
- A Phase 3b, Randomized, Open-Label Study to Evaluate the Safety and Immunogenicity of Select Travel Vaccines When Administered Concomitantly With MenACWY in Adults
- A Phase Ib/II Study of the Safety and Immunogenicity of the Candidate Rabies Vaccine ChAdOx2 RabG
- A Phase II Trial of a Recombinant Human Anti-Rabies Virus Monoclonal Antibody
- A Phase III Clinical Study to Evaluate SYN023's Efficacy and Safety
- A Safety Study of IMOVAX Polio Vaccine in Selected Cities in China
- A Study of RBI-4000 in Healthy Participants
- A Study of the Safety of IMOVAX Polio™ in China
- A Study to Assess the Safety, Reactogenicity and Immune Response of CureVac's Candidate Rabies mRNA Vaccine in Healthy Adults
- [A Study to Evaluate a PIKA Rabies Vaccine（Vero Cell）for Human Use,Freeze-dried](https://trialight.com/data/trial/a-study-to-evaluate-a-pika-rabies-vaccine-vero-cell-for-d8878797-8a33-4e8c-a655-425939e0fa58.md)
- A Study to Evaluate the One Year Long-term Persistence of Immune Responses Following Two Different Rabies Vaccine Post-exposure Regimens in Chinese Children
- A Study to Evaluate the Safety and Immunogenicity of GlaxoSmithKline (GSK) Biologicals' Experimental Rabies Vaccine in Healthy Adults
- A Study to Test Experimental Blood Stage Malaria Vaccine in Burkina Faso.
- A Trial of a Peptide-based Group A Streptococcal (GAS) Vaccine Candidate in Healthy Individuals.
- Antibody Production in Immune Disorders

### In development for (4)

- [HIV infectious disease](https://trialight.com/data/condition/hiv-infectious-disease-1260f28c-d667-55f9-b221-15d5017fde05.md) Phase 2
- [Malaria](https://trialight.com/data/condition/malaria-54828cac-9b96-5833-93e2-e012d4505853.md) Phase 3
- [Plasmodium falciparum malaria](https://trialight.com/data/condition/plasmodium-falciparum-malaria-5e0103dd-4e60-581d-924b-3435883b51f8.md) Phase 2
- Rhabdoviridae infectious disease Phase 3

---

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