Live, attenuated, dengue serotype 1, 2, 3, 4 virus + Placebo: (NaCl) 0.9% solution

Phase 3Completed

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Hype Score

Development Stage

✓

Pre-clinical

✓

Phase 1

✓

Phase 2

Phase 3

Approved

Indication / Disease

Dengue Fever

Conditions

Dengue Fever, Dengue Hemorrhagic Fever, Dengue

Trial Timeline

Jun 8, 2011 → Mar 5, 2018

NCT ID

NCT01374516

About Live, attenuated, dengue serotype 1, 2, 3, 4 virus + Placebo: (NaCl) 0.9% solution

Live, attenuated, dengue serotype 1, 2, 3, 4 virus + Placebo: (NaCl) 0.9% solution is a phase 3 stage product being developed by Sanofi for Dengue Fever. The current trial status is completed. This product is registered under clinical trial identifier NCT01374516. Target conditions include Dengue Fever, Dengue Hemorrhagic Fever, Dengue.

Hype Score Breakdown

Clinical

Activity

Company

Novelty

Community

Clinical Trials (1)

NCT ID	Phase	Status	Start	Completion	Indication
NCT01374516	Phase 3	Completed	Jun 8, 2011	Mar 5, 2018	Dengue Fever

Competing Products

20 competing products in Dengue Fever

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Product	Company	Stage	Hype Score
V180 + Alhydrogel™ + Placebo	Merck	Phase 1	33
Low-dose V180 with low-dose ISCOMATRIX™ adjuvant + Low-dose V180 with medium-dose ISCOMATRIX™ adjuvant + Medium-dose V180 (non-adjuvanted) + Medium-dose V180 with low-dose ISCOMATRIX™ adjuvant + Medium-dose V180 with medium-dose ISCOMATRIX™ adjuvant + Medium-dose V180 with Alhydrogel™ adjuvant + High-dose V180 (non-adjuvanted) + High-dose V180 with low-dose ISCOMATRIX™ adjuvant + High-dose V180 with medium-dose ISCOMATRIX™ adjuvant + Low-dose V180 with high-dose ISCOMATRIX™ adjuvant + Medium-dose V180 with high-dose ISCOMATRIX™ adjuvant + High-dose V180 with high-dose ISCOMATRIX™ adjuvant + Placebo	Merck	Phase 1	33
V181 + Butantan - DV	Merck	Phase 2	52
V181 High-Potency Level + V181 Mid-Potency Level + V181 Low-Potency Level + Placebo	Merck	Phase 2	52
EYU688 + Placebo	Novartis	Phase 2	52
balapiravir [RO4588161] + placebo	Roche	Phase 1	33
Dengue Tetravalent Vaccine, Live	Sanofi	Pre-clinical	22
CYD Dengue Vaccine (5-dose formulation) + Placebo, NaCl 0.9%	Sanofi	Phase 2	51
Chimeric dengue serotype (1, 2, 3, 4) + Chimeric dengue serotype (1, 2, 3, 4) + Chimeric dengue serotype (1, 2, 3, 4)	Sanofi	Phase 2	51
Live, attenuated, recombinant dengue serotypes 1, 2, 3, & 4 virus + Live, attenuated, recombinant dengue serotypes 1, 2, 3, & 4 virus + Live, attenuated, recombinant dengue serotypes 1, 2, 3, & 4 virus + Live, attenuated, recombinant dengue serotypes 1, 2, 3, & 4 virus + Placebo: NaCl 0.9%	Sanofi	Phase 3	76
Live, attenuated, recombinant dengue serotype 1 , 2, 3 , and 4 virus + NaCl 0.9% + Tetanus toxoid, reduced diphtheria toxoid, acellular pertussis vaccine adsorbed + Meningococcal A+C vaccine	Sanofi	Phase 2	51
Live, attenuated, recombinant dengue serotypes 1, 2, 3, and 4 virus + Live, attenuated, recombinant dengue serotypes 1, 2, 3, and 4 virus + Live, attenuated, recombinant dengue serotypes 1, 2, 3, and 4 virus + Yellow Fever	Sanofi	Phase 2	51
Tetravalent CYD Dengue Vaccine , 5555 formulation + Tetravalent CYD Dengue Vaccine , 5553 formulation + Tetravalent CYD Dengue Vaccine, 4444 formulation	Sanofi	Phase 2	51
CYD Dengue Vaccine + Tdap: Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine adsorbed + Tdap: Tetanus toxoid, reduced diphtheria toxoid and acellular pertussis vaccine adsorbed	Sanofi	Phase 3	76
Live, attenuated, recombinant dengue serotypes 1, 2, 3, and 4 virus + Placebo: NaCl 0.9%	Sanofi	Phase 3	76
CYD Dengue Vaccine + CYD Dengue Vaccine + Human Papillomavirus Quadrivalent [Types 6, 11, 16, and 18] Vaccine, Recombinant.	Sanofi	Phase 3	76
CYD dengue vaccine serotypes (1, 2, 3, 4). + Meningococcal Polysaccharide A+C; NaCl; Typhoid Vi polysaccharide	Sanofi	Phase 2	51
CYD Dengue Vaccine + Placebo (Sodium chloride 0.9%)	Sanofi	Phase 2	51
CYD Dengue Vaccine + Inactivated rabies virus vaccine + Placebo	Sanofi	Phase 2	51
Live, attenuated, dengue serotype 1, 2, 3, 4 virus + Placebo: Sodium chloride (NaCl) 0.9%	Sanofi	Phase 3	76

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