General Information of Drug (ID: DM3QDA6)

Drug Name
Polynoma-1 Drug Info
Synonyms Polyvalent melanoma vaccine, Vaccinoma
Indication
Disease Entry ICD 11 Status REF
Melanoma 2C30 Phase 2 [1]
Cross-matching ID
TTD Drug ID
DM3QDA6

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Clinical Trial Drug(s)
Discontinued Drug(s)
Approved Drug(s)
Patented Agent(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Astuprotimut-R DMLY0H5 Non-small-cell lung cancer 2C25.Y Phase 3 [2]
IDM-2101 DMABRXY Colorectal cancer 2B91.Z Phase 2 [3]
GL-0817 DM17OZM Head and neck cancer 2D42 Phase 2 [4]
KITE-718 DMBSI6Y Solid tumour/cancer 2A00-2F9Z Phase 1 [5]
Melanoma vaccine (ALVAC) DM3HIQY Melanoma 2C30 Discontinued in Phase 2 [6]
Drug Name Drug ID Indication ICD 11 Highest Status REF
Multi-epitope peptide melanoma vaccine DMZPEHY Melanoma 2C30 Phase 3 [7]
Melanoma vaccine DMQEC6Z Melanoma 2C30 Phase 3 [8]
MKC-1106-MT DMXKOW6 Melanoma 2C30 Phase 2 [9]
Melanoma vaccine (ALVAC) DM3HIQY Melanoma 2C30 Discontinued in Phase 2 [6]
F-50040 DMMG6W5 Melanoma 2C30 Discontinued in Phase 1 [10]
Drug(s) Targeting Tyrosinase (TYR)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Hydroquinone DM6AVR4 Melasma ED60.1 Approved [11]
Monobenzone DMVJS2K Vitiligo ED63.0 Approved [11]
Multi-epitope peptide melanoma vaccine DMZPEHY Melanoma 2C30 Phase 3 [7]
Melanoma vaccine DMQEC6Z Melanoma 2C30 Phase 3 [8]
MKC-1106-MT DMXKOW6 Melanoma 2C30 Phase 2 [9]
Multi-epitope tyrosinase/gp100 vaccine DMN68ZL Melanoma 2C30 Phase 2 [12]
PMID29130358-Compound-Figure11(3) DMSME2B N. A. N. A. Patented [13]
Benzothiazole analog 1 DMHXFCQ Albinism EC23.2 Patented [14]
Monoamine derivative 2 DMAZ6DI Albinism EC23.2 Patented [14]
Benzimidazole derivative 3 DMY93WG Albinism EC23.2 Patented [14]
⏷ 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
MART-1 melanoma antigen (MLANA) TT362RB MAR1_HUMAN Not Available [1]
Melanoma-associated antigen 3 (MAGEA3) TTWSKHD MAGA3_HUMAN Not Available [1]
Tyrosinase (TYR) TTULVH8 TYRO_HUMAN Not Available [1]

References

1 An immuno-oncology company developing a novel polyvalent antigen therapy for the treatment of melanoma. Polynoma. 2015.
2 National Cancer Institute Drug Dictionary (drug id 600553).
3 Induction of immune responses and clinical efficacy in a phase II trial of IDM-2101, a 10-epitope cytotoxic T-lymphocyte vaccine, in metastatic non-small-cell lung cancer. J Clin Oncol. 2008 Sep 20;26(27):4418-25.
4 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
5 ClinicalTrials.gov (NCT03139370) Safety and Efficacy of MAGE-A3/A6 T Cell Receptor Engineered T Cells (KITE-718) in HLA-DPB1*04:01 Positive Adults With Advanced Cancers. U.S. National Institutes of Health.
6 Preclinical qualification of a new multi-antigen candidate vaccine for metastatic melanoma. J Immunother. 2010 Oct;33(8):743-58.
7 Safety and immunogenicity of vaccination with MART-1 (26-35, 27L), gp100 (209-217, 210M), and tyrosinase (368-376, 370D) in-adjuvant with PF-3512676 and GM-CSF in metastatic melanoma. Correction in: volume 35 on page 650.
8 National Cancer Institute Drug Dictionary (drug id 685201).
9 Interpreting expression profiles of cancers by genome-wide survey of breadth of expression in normal tissues. Genomics 2005 Aug;86(2):127-41.
10 Stability and CTL-activity of P40/ELA melanoma vaccine candidate. Biologicals. 2001 Sep-Dec;29(3-4):293-8.
11 Identification of an Alkylhydroquinone from Rhus succedanea as an Inhibitor of Tyrosinase and Melanogenesis. J Agric Food Chem. 2009 Mar 25;57(6):2200-5.
12 ClinicalTrials.gov (NCT00003362) Vaccine Therapy Plus Immune Adjuvants in Treating Patients With Advanced Melanoma. U.S. National Institutes of Health.
13 Gelatinase inhibitors: a patent review (2011-2017).Expert Opin Ther Pat. 2018 Jan;28(1):31-46.
14 Tyrosinase inhibitors: a patent review (2011-2015).Expert Opin Ther Pat. 2016;26(3):347-62.