General Information of Drug (ID: DMSWZNU)

Drug Name
RO7443904 Drug Info
Synonyms RG6333
Indication
Disease Entry ICD 11 Status REF
Non-hodgkin lymphoma 2B33.5 Phase 1 [1]
Cross-matching ID
TTD Drug ID
DMSWZNU

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Approved Drug(s)
Clinical Trial Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Tisagenlecleucel DMM9BJD Acute lymphoblastic leukaemia 2A85 Approved [3]
Blinatumomab DMGECIJ Acute lymphoblastic leukaemia 2A85 Approved [4]
Axicabtagene ciloleucel DMYHN59 Diffuse large B-cell lymphoma 2A81 Approved [5]
Lisocabtagene maraleucel DMP45ME Large B-cell lymphoma 2A81 Approved [6]
Inebilizumab DMI0RHA Neuromyelitis optica spectrum disorder 8E4A.0 Approved [7]
Tecartus DMYQCWT Mantle cell lymphoma 2A85.5 Approved [8]
Loncastuximab tesirine DMXSVGI Diffuse large B-cell lymphoma 2A81 Approved [9]
Obexelimab DMVIC4J IgG4 related disease 4A43.0 Phase 3 [10]
MOR-208 DMDQOWT Diffuse large B-cell lymphoma 2A81 Phase 2/3 [11]
CART-19 DMST3FM Acute lymphoblastic leukaemia 2A85 Phase 2/3 [12]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Belatacept DMXLYQF Kidney transplant rejection NE84 Approved [13]
AB-103 DMPDQ8T Necrotizing soft tissue infection 1B71 Phase 3 [14]
Lulizumab pegol DMGWZ93 Systemic lupus erythematosus 4A40.0 Phase 2 [15]
REGN5678 DM0Y6WU Prostate cancer 2C82.0 Phase 1/2 [16]
AU101 DMLAKPI Osteosarcoma 2B51 Phase 1/2 [17]
REGN5668 DMH1UV5 Ovarian cancer 2C73 Phase 1/2 [18]
SAR442257 DMXD5QP Malignant neoplasm 2A00-2F9Z Phase 1 [19]
CD28 and CD137 CAR-T Cells DMFGQXB Acute lymphoblastic leukaemia 2A85 Phase 1 [20]
CD19-CAR and CD28-CAR T Cells DMUR1MN Acute lymphoblastic leukaemia 2A85 Phase 1 [21]
RG6333 DM1BRF2 Non-hodgkin lymphoma 2B33.5 Phase 1 [22]
⏷ Show the Full List of 10 Drug(s)

Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
B-lymphocyte surface antigen B4 (CD19) TTW640A CD19_HUMAN Not Available [2]
T-cell-specific surface glycoprotein CD28 (CD28) TTQ13FT CD28_HUMAN Not Available [2]

References

1 ClinicalTrials.gov (NCT05219513) An Open-Label, Phase 1 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of RO7443904 in Combination With Glofitamab in Participants With Relapsed/Refractory B-Cell Non-Hodgkin's Lymphoma. U.S.National Institutes of Health.
2 Clinical pipeline report, company report or official report of Genentch
3 2017 FDA drug approvals.Nat Rev Drug Discov. 2018 Feb;17(2):81-85.
4 2014 FDA drug approvals. Nat Rev Drug Discov. 2015 Feb;14(2):77-81.
5 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services
6 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services.
7 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2020
8 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services.
9 Final results of a phase 1 study of loncastuximab tesirine in relapsed/refractory B-cell non-Hodgkin lymphoma. Blood. 2021 May 13;137(19):2634-2645.
10 Emerging B-Cell Therapies in Systemic Lupus Erythematosus. Ther Clin Risk Manag. 2021 Jan 14;17:39-54.
11 A phase 1 trial of the Fc-engineered CD19 antibody XmAb5574 (MOR00208) demonstrates safety and preliminary efficacy in relapsed CLL. Blood. 2014 Dec 4;124(24):3553-60.
12 ClinicalTrials.gov (NCT03027739) CART-19 Cells For MRD Positive CD19+ ALL
13 New developments in immunosuppressive therapy for heart transplantation. Expert Opin Emerg Drugs. 2009 Mar;14(1):1-21.
14 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
15 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
16 Clinical pipeline report, company report or official report of Regeneron Pharmaceuticals.
17 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
18 ClinicalTrials.gov (NCT04590326) Phase 1/2 Study of REGN5668 (MUC16xCD28, a Costimulatory Bispecific) Administered in Combination With Cemiplimab or REGN4018 (MUC16xCD3). U.S.National Institutes of Health.
19 Clinical pipeline report, company report or official report of Sanofi.
20 ClinicalTrials.gov (NCT02186860) Chimeric Antigen Receptor (CAR)-Modified T Cell Therapy in Treating Patients With Acute Lymphoblastic Leukemia
21 ClinicalTrials.gov (NCT02146924) Cellular Immunotherapy in Treating Patients With High-Risk Acute Lymphoblastic Leukemia
22 Clinical pipeline report, company report or official report of Roche