BiologicalDrug
TLR4 Agonist G100 clinical trials
- studies test it
- 13
- open now
- 0
- in phase 3
- 0
- first study started
- 2011
How studies write it
Studies that test it under each name
Name
- GLA-SE
- 10
Combined with it in one product
Studies by the year they started
13 studies that test it; most in 2014 (3)
| Year | Studies |
|---|---|
| 2011 | 1 |
| 2012 | 2 |
| 2013 | 1 |
| 2014 | 3 |
| 2015 | 2 |
| 2016 | 3 |
| 2019 | 1 |
By phase
A phase 1/2 study counts in both.
- Early Phase 1
- 1
- Phase 1
- 11
- Phase 2
- 1
What it is tested for
Each study’s main condition, where its own words name it.
Who runs them
Industry 1 · Other 12
Access to Advanced Health Institute (AAHI) (3) · National Institute of Allergy and Infectious Diseases (NIAID) (2) · Institut National de la Santé Et de la Recherche Médicale, France (1) · Mayo Clinic (1) · Fred Hutchinson Cancer Center (1) · University Hospital Tuebingen (1) · Immune Design, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA) (1) · Oswaldo Cruz Foundation (1)
Often tested with
Tested in the same studies.
Aluminum Hydroxide (2) · LEISH-F3 (2) · Gla-af (2) · EM060G (1) · Nivolumab (1) · Ipilimumab (1)
Studies
Open first, then newest update. How each study uses TLR4 Agonist G100 is read from its arms, and is right about nine times in ten.
Testing it · 13
- Trial to Evaluate the Safety and Immunogenicity of a Placental Malaria Vaccine Candidate (PRIMVAC ) in Healthy AdultsCompletedPhase 1Institut National de la Santé Et de la Recherche Médicale, FranceNCT02658253Written as GLA-SE
- Study of Intratumoral Ipilimumab and TLR4 Agonist GLA-SE in Combination With Systemic Nivolumab and ChemotherapyWithdrawnPhase 1Gustave Roussy, Cancer Campus, Grand ParisNCT03982121Written as GLA-SE
- MART-1 Antigen With or Without TLR4 Agonist GLA-SE in Treating Patients With Stage II-IV Melanoma That Has Been Removed by SurgeryCompletedEarly Phase 1Mayo ClinicNCT02320305Written as TLR4 Agonist GLA-SE
- TLR4 Agonist GLA-SE and Radiation Therapy in Treating Patients With Soft Tissue Sarcoma That Is Metastatic or Cannot Be Removed by SurgeryCompletedPhase 1Fred Hutchinson Cancer CenterNCT02180698Written as TLR4 Agonist GLA-SE
- Safety and Immunogenicity of the Placental Malaria Vaccine Candidate PAMVAC Variously AdjuvantedCompletedPhase 1University Hospital TuebingenNCT02647489Written as GLA-SE
- A Proof-of-Concept Trial of GLA-SE in Patients With Merkel Cell CarcinomaCompletedPhase 1Immune Design, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)NCT02035657Written as GLA-SE
- Study of Safety and Immune Response of the Sm14 Vaccine in Adults of Endemic RegionsCompletedPhase 2Oswaldo Cruz FoundationNCT03041766Written as GLA-SE solution
- Safety, Tolerability, and Immunogenicity of the Vaccine Candidates ID93 + AP10-602 and ID93 + GLA-SE Administered Intramuscularly in Healthy Adult SubjectsCompletedPhase 1National Institute of Allergy and Infectious Diseases (NIAID)NCT02508376Written as GLA-SE
- LEISH-F3 + GLA-SE and the LEISH-F3 + MPL-SE VaccineCompletedPhase 1National Institute of Allergy and Infectious Diseases (NIAID)NCT01751048Written as GLA-SE
- Phase 1 LEISH-F3 + SLA-SE Vaccine Trial in Healthy Adult VolunteersCompletedPhase 1Access to Advanced Health Institute (AAHI)NCT02071758Written as LEISH-F3 + GLA-SE
- The Effects of GLA (5 mcg) on Human VolunteersCompletedPhase 1Access to Advanced Health Institute (AAHI)NCT01864876Written as GLA-SE
- Phase 1 LEISH-F3 Vaccine Trial in Healthy Adult VolunteersCompletedPhase 1Access to Advanced Health Institute (AAHI)NCT01484548Written as LEISH-F3 + GLA-SE
- The Effects of GLA on Human VolunteersCompletedPhase 1Rockefeller UniversityNCT01397604Written as GLA-SE
Given in every arm · 4 — TLR4 Agonist G100 is usual care beside what is tested
- A Clinical Trial in Healthy, HIV-1-Uninfected Adult Participants to Compare the Safety, Tolerability and Immunogenicity of CH505TF gp120 Produced From Stably Transfected Cells to CH505TF gp120 Produced From Transiently Transfected CellsCompletedPhase 1National Institute of Allergy and Infectious Diseases (NIAID)NCT03856996Written as Glucopyranosyl Lipid Adjuvant-Stable Emulsion (GLA-SE)
- Study of Intratumoral G100 With Or Without Pembrolizumab or Rituximab In Participants With Follicular Non-Hodgkin's Lymphoma (MK-3475-174/IMDZ-G142)TerminatedPhase 1/2Immune Design, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)NCT02501473Written as G100
- Phase 1b Safety Study of CMB305 in Patients With Locally Advanced, Relapsed, or Metastatic Cancer Expressing NY-ESO-1TerminatedPhase 1Immune Design, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)NCT02387125Written as G100
- Anti-Schistosomiasis Vaccine: Sm14 Phase 2b-Sn in School ChildrenCompletedPhase 2Oswaldo Cruz FoundationNCT03799510Written as GLA-SE solution