2
Indication details
- Control Arm
- Single arm
- Therapeutic Indication
- Treatment for adult patients with unresectable or metastatic melanoma previously treated with a PD-1 blocking antibody, and if BRAF V600 positive, a BRAF inhibitor with or without a MEK inhibitor.
- Tumour Type
-
Skin Cancers
- Tumour Sub-type
- Melanoma
- Tumour Stage
- Unresectable or metastatic
- Trial Name
- LN-144
- NCT Number
- NCT02360579
- Trial Phase
- Phase II
Approval details
- FDA Approval
- FDA accelerated approval February 2024
Primary Outcome(s)
- Primary Outcome(s)
- ORR and DOR
- Evaluated Outcome
- ORR
- Form(s)
- Form 3
Outcome Data
- ORR
- 31.40%
- DoR
- >9 months
Adjustments
- QoL Comment
-
QoL was not a prespecified endpoint
- Toxicity Comment
-
41.7% febrile neutropenia grade 3/4
Score (after adjustments)
- Preliminary non-curative score
-
3
- Toxicity adjustment
- -1
- Non-curative score
-
2
Scorecard details
- ESMO-MCBS version
- ESMO-MCBS v1.1
- Scorecard ID
- 430
- Scorecard version
- 1
- Issue date
- 22.03.2024
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: