2
Indication details
- Control Arm
- Single arm (Phase I/II)
- FDA Therapeutic Indication
- Treatment for adult patients with metastatic triple-negative breast cancer who received at least two prior therapies for metastatic disease
- Tumour Sub-type
- Breast Cancer
- Tumour Stage
- Metastatic
- Tumour Sub-Group
- Triple-negative
- Trial Name
- IMMU-132-01
- NCT Number
- NCT01631552
- Trial Phase
- Phase I/II
Approval details
- FDA Approval
- FDA approval April 2020
- EMA Approval
- EMA (CHMP) October 2021 EC decision December 2021
Primary Outcome(s)
- Primary Outcome(s)
- ORR
- Evaluated Outcome
- ORR, DOR
- Form(s)
- Form 3
Outcome Data
- PFS Control
- 5.5 months
- ORR
- 33.3%
- DoR
- 7.7 months
Adjustments
- QoL Comment
-
Not qualified for an ESMO-MCBS credit
Score (after adjustments)
- Preliminary non-curative score
-
2
- Non-curative score
-
2
- Comment
-
FDA approval April 2020
Scorecard details
- ESMO-MCBS version
- ESMO-MCBS v1.1
- Scorecard ID
- 224
- Scorecard version
- 1
- Issue date
- 4.11.2020
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: