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Trametinib

Phase 2

Grade 1 Glioma | Small molecule | Oncology |Pulmonx Corporation|Last Updated: Aug 20, 2026

Target and mechanism

Molecular targetMAP2K2, MAP2K1
Target classInhibitor
ModalitySmall molecule

Success Probability

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Market & Valuation

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Trial Design

RandomizedACTIVE_CONTROLLEDDMCBiomarker
Total Trials1
Total Enrollment134

FDA Designations

No designations recorded

Clinical trial landscape

Trametinib · 1 trial · 3 indications

Phase 2 1
NCT05180825Pediatric Low Grade Glioma - MEKinhibitor TRIal vs ChemotherapyGrade 1 Glioma
RECRUITING134 Analytics
PHASE2RECRUITING
Pediatric Low Grade Glioma - MEKinhibitor TRIal vs Chemotherapy
Grade 1 GliomaUnlock trial analytics

Study Endpoints

Primary Endpoints

The primary endpoint is the 3-year PFS (Progression Free Survival rates) comparing the two arms (standard vs experimental).
At 3 years

Secondary Endpoints

the OS rate:
At 3 years
the tumor response based on the international and recognized RANO criteria,
at 24 weeks
the frequency and description of AE (adverse event)/SAE (serious adverse event)
At the end of Cycle 18 (each cycle is 28 days)
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Study Design & Arms

AllocationRANDOMIZED
MaskingNONE
ModelPARALLEL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
Trametinib experimental armEXPERIMENTALthe experimental arm will be Mekinist© (Trametinib) taken orally each day with a 18-course schedule of 4 weeks each.
Vinblastine control armACTIVE_COMPARATORthe control arm will be the weekly intra-venous Vinblastine (Velbe©) during 18 courses of 4 weeks each

Interventions

NameTypeDescription
TrametinibDRUGMekinist© (Trametinib) taken orally each day with a 18-course schedule of 4 weeks each.
VinblastineDRUGweekly intra-venous Vinblastine (Velbe©) during 18 courses of 4 weeks each
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Eligibility Criteria

Age Range1 Month to 25 Years
SexALL
Healthy VolunteersNo
Study Sites25

Inclusion Criteria: * Age: ≥ 1 month to ≤ 25 years * Signed written informed consent prior to study participation of the legal representatives and the patient if the patient can understand the impact of clinical trial and to give consent. For patients above 18 years, their written informed consent ...

Countries:France
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