3
Indication details
- Control Arm
- Single arm
- Therapeutic Indication
- Mirdametinib for adult and pediatric patients 2 years of age and older with neurofibromatosis type 1 (NF1) who have symptomatic plexiform neurofibromas (PN) not amenable to complete resection.
- Tumour Type
-
Non-cancerous soft-tissue tumour
- Tumour Sub-type
- Plexiform neurofibromas (PN) associated with Neurofibromatosis Type 1 (NF1)
- Tumour Sub-Group
- NF1
- Trial Name
- ReNeu
- NCT Number
- NCT03962543
- Trial Phase
- Phase II
Approval details
- FDA Approval
- FDA approval February 2025
Primary Outcome(s)
- Primary Outcome(s)
- ORR
- Evaluated Outcome
- ORR
- Form(s)
- Form 3
Outcome Data
- ORR
- 41%
- DoR
- NR, ≥ 9 months
Adjustments
- QoL Comment
-
Reviewed, but not qualified for an ESMO-MCBS credit
Score (after adjustments)
- Preliminary non-curative score
-
3
- Non-curative score
-
3
Scorecard details
- ESMO-MCBS version
- ESMO-MCBS v1.1
- Scorecard ID
- 492
- Scorecard version
- 1
- Issue date
- 04.04.2025
- Last update
- 28.04.2025
Legend
Information about symbols, abbrevations and color codes
- DFS
- Disease-Free Survival
- DoR
- Duration of Response
- EFS
- Event-Free Survival
- HR
- Hazard Ratio
- NEB
- No evaluable benefit
- NI
- Non-inferiority Study
- ORR
- Overall Response Rate
- OS
- Overall Surival
- pCR
- Pathological Complete Response/Remission
- PFS
- Progression-Free Survival
- QoL
- Quality of Life
- RFS
- Relapse-Free Survival
- RR
- Response Rate
QoL adjustments
Other adjustments*
Serious and disabling adverse effects
Red = negative / deterioration
Green = positive / improvement
Red = negative / deterioration
Green = positive / improvement
Red = negative / deterioration
Green = positive / improvement
Red = negative / deterioration
Green = positive / improvement
* Other adjustments include: