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Chikungunya

9 published articles · Updated continuously

Clinical Trial Landscape

Clinical Trials for Chikungunya

19 trials tracked for Chikungunya: 4 in phase 3 or 4 and 3 with published results. The most-cited published study has 231 citations.

19Trials tracked
4Phase 3 & 4
0Recruiting
3With published results
Phase distribution
Phase 3 4 Phase 2 8 Phase 1 3 Other / NA 4
  1. Phase 3 Pivotal Study to Evaluate Safety and Immunogenicity of a Live-Attenuated Chikungunya Virus Vaccine Candidate in Adults Completed · 231 cited
  2. Phase 3 A Phase 3 Trial of the VLP-Based Chikungunya Vaccine PXVX0317 (CHIKV VLP Vaccine) Completed · 78 cited
  3. Phase 3 Safety and Immunogenicity of CHIKV VLP Vaccine PXVX0317 in Adults ≥65 Years Completed · 78 cited
  4. Phase 3 Study to Demonstrate Consistency of Three Lots of a Live-attenuated Chikungunya Virus Vaccine Candidate in Healthy Adults Completed
  5. Phase 2 A Study to Assess the Safety and Immunogenicity of PXVX0317 Chikungunya Virus Virus-Like Particle Vaccine Completed
  6. Phase 2 Phase 2 Open-label Study of Alum-adjuvanted Chikungunya Virus-like Particle Vaccine (PXVX0317) Completed
Show 13 more trials
  1. Phase 2 Chikungunya Vaccine (V184) Study in Previously Exposed Adults (V184-006) Completed
  2. Phase 2 Trial of a Chikungunya Vaccine, PXVX0317 CHIKV-VLP, in Healthy Adults Completed
  3. Phase 2 Trial for Safety and Immunogenicity of a Chikungunya Vaccine, VRC-CHKVLP059-00-VP, in Healthy Adults Completed
  4. Phase 2 Study of a Live Attenuated Chikungunya Vaccine in a Previously Epidemic Area Completed
  5. Phase 2 Phase II Study to Evaluate Safety and Immunogenicity of a Chikungunya Vaccine Completed
  6. Phase 2 Safety, Tolerability and Long-term Immunogenicity of Different Formulations of a Chikungunya Vaccine (V184-005) Completed
  7. Phase 1 Safety, Tolerability, and Immunogenicity of VAL-181388 in Healthy Participants Completed
  8. Phase 1 Chikungunya Virus Vaccine Trial in Healthy Adults Completed
  9. Phase 1 Phase 1 Study of SAR440894 vs Placebo Completed
  10. N/A A Prospective, Open Label, Treatment Use Study of Patient Safety Following Transfusion of INTERCEPT Platelet Components Completed
  11. N/A Quantifying the Epidemiological Impact of Targeted Indoor Residual Spraying on Aedes-borne Diseases Completed
  12. N/A Defining Skin Immunity of a Bite of Key Insect Vectors in Humans Completed
  13. N/A Sylvatic Transmission of Zika, Dengue, and Chikungunya Viruses in Thailand and Cambodia Completed

Showing the 19 most-cited and recently-updated of 19 trials. Browse the full registry →

Trial data sourced from ClinicalTrials.gov. Counts describe the research landscape and are not a treatment recommendation. Informational only — not medical advice.

What the trials found For clinicians

Chikungunya: what the trials found

Several vaccine candidates demonstrate significant immunogenicity against Chikungunya. The VLA1553 vaccine showed a fold increase in CHIKV-specific neutralizing antibody titers compared to baseline (1.02, 1.00, 1.08, and 1.00) with specific cohorts showing much higher increases (up to 460.27 or 399.91) [1, 4]. Additionally, the VRC-CHKVLP059-00-VP vaccine was evaluated for reactogenicity; local and systemic signs were reported in various groups following administration [12, 15].

The CHIKV VLP/adjuvant platform demonstrated high seroresponse rates. Specifically, anti-CHIKV SNA seroresponse rates at Day 22 reached 87.3% 2 and 97.81% 3, with corresponding Geometric Mean Titers (GMT) of 724 2 and 1618 3. These trials also observed high seroresponse rates at other time points, such as Day 15 (82.3% 2; 96.8% 3) and Day 183 (75.5% 3).

Recent results — preliminary, needs further review

  • The SAR440894 vaccine was evaluated in a Phase 1 trial 13.
  • Targeted Indoor Residual Spraying (TIRS) was evaluated as an intervention 16.

For the clinician treating this condition

  • Multiple VLP-based and adjuvanted formulations show high seroresponse rates and significant neutralizing antibody titers against Chikungunya.
  • Clinical data for the VLA1553 vaccine confirms both immunogenicity (neutralizing antibody fold increases) and safety profiles regarding unsolicited adverse events.
  • Reactogenicity data is available for the VRC-CHKVLP059-00-VP candidate to inform expectations on local and systemic responses.

AI synthesis of 4 cited trials, updated Jun 19, 2026. Informational only — not medical advice; trial data sourced from ClinicalTrials.gov. How we use AI.

HCP Mode — summaries include clinical detail, trial data, and statistical outcomes.
Patient Mode — summaries use plain language, avoiding clinical jargon.

Questions about Chikungunya

Can a narrative review tell me about Chikungunya virus infection outcomes?

A narrative review explains the immune mechanisms behind Chikungunya but does not provide specific clinical outcome data like infection rates or long-term recovery statistics.

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Is the new chikungunya vaccine safe for my young child?

A Phase 3 trial is currently testing a new chikungunya vaccine for children aged 1 to 12 years to evaluate its safety and ability to build immunity.

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How does climate change affect chikungunya outbreaks in my area?

Climate change expands the habitats of mosquitoes that carry chikungunya, allowing outbreaks to occur in new areas and during longer seasons.

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