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Nemtabrutinib

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Sevindik, Ömür Gökmen; Chen, Chang; Yang, Jing; Farooqui, Mohammed Z.H.; Paszkiewicz-Kozik, Ewa (1 June 2023). "BELLWAVE-008: A phase 3 study of the efficacy and safety of nemtabrutinib in previously untreated patients (pts) with chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL)
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Woyach, Jennifer A.; Stephens, Deborah M.; Flinn, Ian W.; Bhat, Seema A.; Savage, Ronald E.; Chai, Feng; Eathiraj, Sudharshan; Reiff, Sean D.; Muhowski, Elizabeth M.; Granlund, Lindsey; Szuszkiewicz, Lyndsey; Wang, Wayne; Schwartz, Brian; Ghori, Razi; Farooqui, Mohammed Z. H.; Byrd, John C. (6
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Reiff, Sean D.; Mantel, Rose; Smith, Lisa L.; Greene, J.T.; Muhowski, Elizabeth M.; Fabian, Catherine A.; Goettl, Virginia M.; Tran, Minh; Harrington, Bonnie K.; Rogers, Kerry A.; Awan, Farrukh T.; Maddocks, Kami; Andritsos, Leslie; Lehman, Amy M.; Sampath, Deepa; Lapalombella, Rosa; Eathiraj,
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Woyach, Jennifer A.; Flinn, Ian W.; Awan, Farrukh T.; Eradat, Herbert; Brander, Danielle; Tees, Michael; Parikh, Sameer A.; Phillips, Tycel J.; Ghori, Razi; Reddy, Nishitha M.; Farooqui, Mohammed Z.H.; Byrd, John C.; Stephens, Deborah M. (15 November 2022).
355:"Efficacy and Safety of Nemtabrutinib, a Wild-Type and C481S-Mutated Bruton Tyrosine Kinase Inhibitor for B-Cell Malignancies: Updated Analysis of the Open-Label Phase 1/2 Dose-Expansion Bellwave-001 Study" 261:"P682: Nemtabrutinib (Mk-1026), A Non-Covalent Inhibitor of Wild-Type and C481S Mutated Bruton Tyrosine Kinase for B-Cell Malignancies: Efficacy and Safety of the Phase 2 Dose-Expansion Bellwave-001 Study" 259:
Woyach, J.; Flinn, I. W.; Awan, F. T.; Eradat, H.; Brander, D.; Tees, M.; Parikh, S. A.; Phillips, T.; Wang, W.; Reddy, N. M.; Farooqui, M. Z.; Byrd, J. C.; Stephens, D. M. (23 June 2022).
397:"First in Human Study of the Reversible BTK Inhibitor Nemtabrutinib in Patients with Relapsed/Refractory Chronic Lymphocytic Leukemia and B-Cell Non-Hodgkin Lymphoma" 540: 559: 54: 564: 301:
Sudharshan; Abbadessa, Giovanni; Schwartz, Brian; Johnson, Amy J.; Byrd, John C.; Woyach, Jennifer A. (1 October 2018).
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paid $ 2.7 billion to acquire the company ArQule and the drug, which is being investigated as a cancer treatment.
584: 533: 579: 569: 574: 526: 75: 475: 428: 376: 282: 241: 467: 420: 412: 334: 202:(BTK) inhibitor; unlike other BTK inhibitors it also works against some mutated forms of BTK. 84: 459: 404: 366: 324: 314: 272: 233: 145: 129: 237: 510: 329: 302: 277: 260: 203: 303:"The BTK Inhibitor ARQ 531 Targets Ibrutinib-Resistant CLL and Richter Transformation" 109: 553: 479: 447: 432: 380: 286: 245: 506: 408: 319: 198:(MK-1026, formerly ARQ 531) is a small molecule drug that works as a reversible 463: 371: 354: 181: 20: 471: 416: 396: 424: 338: 28: 498: 95: 514: 180: 144: 139: 119: 94: 74: 69: 53: 48: 40: 35: 108: 83: 534: 8: 19: 541: 527: 27: 448:"Merck will pay $ 2.7 billion for ArQule" 370: 328: 318: 276: 128: 215: 18: 7: 495: 493: 238:10.1200/JCO.2023.41.16_suppl.TPS7594 446:Lisa m. Jarvis (16 December 2019). 99: 278:10.1097/01.HS9.0000845612.25766.0c 14: 497: 165: 162: 156: 171: 150: 1: 513:. You can help Knowledge by 409:10.1158/2159-8290.CD-23-0670 320:10.1158/2159-8290.CD-17-1409 226:Journal of Clinical Oncology 365:(Supplement 1): 7004–7006. 224:without TP53 aberrations". 606: 560:Tyrosine kinase inhibitors 492: 452:C&EN Global Enterprise 140:Chemical and physical data 464:10.1021/cen-09748-buscon4 372:10.1182/blood-2022-163596 26: 200:Bruton's tyrosine kinase 509:-related article is a 232:(16_suppl): TPS7594. 565:Small-molecule drugs 23: 590:Pharmacology stubs 522: 521: 313:(10): 1300–1315. 193: 192: 16:Chemical compound 597: 585:Pyrrolopyridines 543: 536: 529: 501: 494: 484: 483: 443: 437: 436: 401:Cancer Discovery 395:November 2023). 391: 385: 384: 374: 349: 343: 342: 332: 322: 307:Cancer Discovery 297: 291: 290: 280: 256: 250: 249: 220: 188: 173: 167: 164: 158: 152: 132: 112: 102: 101: 87: 44:MK-1026; ARQ 531 31: 24: 22: 605: 604: 600: 599: 598: 596: 595: 594: 550: 549: 548: 547: 490: 488: 487: 445: 444: 440: 393: 392: 388: 351: 350: 346: 299: 298: 294: 258: 257: 253: 222: 221: 217: 212: 186: 176: 170: 161: 155: 135: 115: 98: 90: 65: 62:Investigational 17: 12: 11: 5: 603: 601: 593: 592: 587: 582: 577: 572: 567: 562: 552: 551: 546: 545: 538: 531: 523: 520: 519: 502: 486: 485: 438: 386: 344: 292: 251: 214: 213: 211: 208: 191: 190: 184: 178: 177: 174: 168: 159: 153: 148: 142: 141: 137: 136: 134: 133: 125: 123: 117: 116: 114: 113: 105: 103: 92: 91: 89: 88: 80: 78: 72: 71: 67: 66: 64: 63: 59: 57: 51: 50: 46: 45: 42: 38: 37: 33: 32: 15: 13: 10: 9: 6: 4: 3: 2: 602: 591: 588: 586: 583: 581: 580:Benzaldehydes 578: 576: 573: 571: 570:Phenol ethers 568: 566: 563: 561: 558: 557: 555: 544: 539: 537: 532: 530: 525: 524: 518: 516: 512: 508: 503: 500: 496: 491: 481: 477: 473: 469: 465: 461: 457: 453: 449: 442: 439: 434: 430: 426: 422: 418: 414: 410: 406: 402: 398: 390: 387: 382: 378: 373: 368: 364: 360: 356: 348: 345: 340: 336: 331: 326: 321: 316: 312: 308: 304: 296: 293: 288: 284: 279: 274: 270: 266: 262: 255: 252: 247: 243: 239: 235: 231: 227: 219: 216: 209: 207: 205: 201: 197: 196:Nemtabrutinib 185: 183: 179: 149: 147: 143: 138: 131: 127: 126: 124: 122: 118: 111: 107: 106: 104: 97: 93: 86: 82: 81: 79: 77: 73: 68: 61: 60: 58: 56: 52: 47: 43: 39: 36:Clinical data 34: 30: 25: 21:Nemtabrutinib 575:Chloroarenes 515:expanding it 507:pharmacology 504: 489: 455: 451: 441: 400: 389: 362: 358: 347: 310: 306: 295: 268: 264: 254: 229: 225: 218: 195: 194: 85:2095393-15-8 55:Legal status 49:Legal status 271:: 578–579. 189: g·mol 70:Identifiers 41:Other names 554:Categories 458:(48): 13. 265:HemaSphere 210:References 182:Molar mass 130:JTZ51LIXN4 76:CAS Number 480:212811804 472:2474-7408 433:265032444 417:2159-8290 381:256785160 287:250001988 246:259080098 110:129045720 425:37930156 339:30093506 330:6261467 146:Formula 96:PubChem 478:  470:  431:  423:  415:  379:  337:  327:  285:  244:  187:478.93 505:This 476:S2CID 429:S2CID 377:S2CID 359:Blood 283:S2CID 242:S2CID 204:Merck 511:stub 468:ISSN 421:PMID 413:ISSN 335:PMID 121:UNII 460:doi 405:doi 367:doi 363:140 325:PMC 315:doi 273:doi 234:doi 100:CID 556:: 474:. 466:. 456:97 454:. 450:. 427:. 419:. 411:. 403:. 399:. 375:. 361:. 357:. 333:. 323:. 309:. 305:. 281:. 267:. 263:. 240:. 230:41 228:. 163:Cl 160:23 154:25 542:e 535:t 528:v 517:. 482:. 462:: 435:. 407:: 383:. 369:: 341:. 317:: 311:8 289:. 275:: 269:6 248:. 236:: 175:4 172:O 169:4 166:N 157:H 151:C

Index


Legal status
CAS Number
2095393-15-8
PubChem
129045720
UNII
JTZ51LIXN4
Formula
Molar mass
Bruton's tyrosine kinase
Merck
doi
10.1200/JCO.2023.41.16_suppl.TPS7594
S2CID
259080098
"P682: Nemtabrutinib (Mk-1026), A Non-Covalent Inhibitor of Wild-Type and C481S Mutated Bruton Tyrosine Kinase for B-Cell Malignancies: Efficacy and Safety of the Phase 2 Dose-Expansion Bellwave-001 Study"
doi
10.1097/01.HS9.0000845612.25766.0c
S2CID
250001988
"The BTK Inhibitor ARQ 531 Targets Ibrutinib-Resistant CLL and Richter Transformation"
doi
10.1158/2159-8290.CD-17-1409
PMC
6261467
PMID
30093506
"Efficacy and Safety of Nemtabrutinib, a Wild-Type and C481S-Mutated Bruton Tyrosine Kinase Inhibitor for B-Cell Malignancies: Updated Analysis of the Open-Label Phase 1/2 Dose-Expansion Bellwave-001 Study"
doi

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