Antibody-drug Conjugate Information
General Information of This Antibody-drug Conjugate (ADC)
| ADC ID |
DRG0GNFMC
|
|||||
|---|---|---|---|---|---|---|
| ADC Name |
LMB-7
|
|||||
| Synonyms |
B3 (Fv) PE 38; LMB 7; LMB-7; LMB7; NSC 658931
Click to Show/Hide
|
|||||
| Organization |
National Cancer Institute
|
|||||
| Drug Status |
Phase 1
|
|||||
| Antibody Name |
Murine mAb B3
|
Antibody Info | ||||
| Antigen Name |
Poly [ADP-ribose] polymerase 1 (PARP1)
|
Antigen Info | ||||
| Payload Name |
Pseudomonas exotoxin PE38
|
Payload Info | ||||
| Therapeutic Target |
Eukaryotic elongation factor 2 kinase (EEF2K)
|
Target Info | ||||
| Linker Name |
Undisclosed
|
|||||
| Conjugate Type |
Random conjugation through reduced inter-chain cysteines.
|
|||||
The indication landscape of This ADC(2027 Update)
The clinical trial pipeline of This ADC(2027 Update)
| Indication | Phase 1 | Phase 1/2 | Phase 2 | Phase 2/3 | Phase 3 | New Drug Application | Approved | ||
|---|---|---|---|---|---|---|---|---|---|
| Brain cancer |
1 Trials
|
General Information of The Activity Data Related to This ADC
Identified from the Human Clinical Data
Full List of Activity Data of This Antibody-drug Conjugate
Identified from the Human Clinical Data
| Experiment 1 Reporting the Activity Date of This ADC | [1] | ||||
| Patients Enrolled |
Key disease criteria include histologically confirmed CNS/extraneural tumors with ≥30% B3 antibody reactivity in CSF/tumor cells. Patient requirements: age ≥18, Karnofsky 50-100%, adequate hematologic/renal/hepatic function
|
||||
| Administration Dosage |
.
|
||||
| Related Clinical Trial | |||||
| NCT Number | NCT00003020 | Clinical Status | PHASE1 | ||
| Clinical Description | Protocol for a Phase I Study of Intrathecal LMB-7 (Single-Chain Immunotoxin Constructed From Monoclonal Antibody B3-Pseudomonas Exotoxin PE 38) [IND 5863, NSC 658931] in the Treatment of Patients With Leptomeningeal Neoplasms | ||||
| Experiment 2 Reporting the Activity Date of This ADC | [2] | ||||
| Patients Enrolled |
Patients with leptomeningeal metastases.
|
||||
| Administration Dosage |
.
|
||||
| Related Clinical Trial | |||||
| NCT Number | NCT00003020 | Clinical Status | Phase 1 | ||
| Clinical Description | Phase 1 dose-escalation study of intravenous CMD-193 in subjects with advanced malignant solid tumors. | ||||
References
