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Alkeran: profile and news
Doxil® in the VAD Regimen for Myeloma Confirmed Less Toxic Than ... Feb 28, 2006 Velcade® plus Melphalan Shows Encouraging Activity in Multiple ... Feb 23, 2006 Treanda TM (Bendamustine) Plus Prednisone Superior to Melphalan ... Jan 27, 2006 Treanda™/Prednisone Superior to Melphalan/Prednisone for ... Jan 30, 2006 Celgene Corporation Reviews Recent Highlights and Outlines 2006 ... Jan 9, 2006 Alkeran®/Prednisone Remains Standard Therapy for Elderly Patients ... Oct 4, 2005 Melphalan/Prednisone Favorable in Multiple Myeloma Patients ... Sep 30, 2005 Celgene halted for FDA vote Sep 14, 2005 FDA panel backs Celgene's cancer drug Sep 14, 2005 Efficacy of High-Dose Chemotherapy with Autologous Stem Cell ... Aug 19, 2005 Case Charging Nation's Largest Drug Companies of Defrauding ... Aug 18, 2005 Spector, Roseman & Kodroff, PC Say Federal Judge Allows Consumers ... Aug 19, 2005 Celgene: A Biotech With Profits And A Pipeline Jul 6, 2005 Desi 'chemists' flying in foreign drugs Jul 12, 2005 Garden State Business Briefs Jun 27, 2005 Celgene: A Biotech With Profits And A Pipeline Jul 6, 2005 Enzyme Stopper Combats Cancers Jun 4, 2005 Celgene Corporation First Quarter Results Deliver Record Operating ... Apr 28, 2005 Celgene Corporation First Quarter Results Deliver Record Operating ... 28 Apr 2005 Anticancer combination shows promise in phase II Apr 12, 2005 Other information Indication Used to treat cancer of the ovaries and a certain type of cancer in the bone marrow Pharmacology Melphalan is an antineoplastic in the class of alkylating agents and is used to treat various forms of cancer. Alkylating agents are so named because of their ability to add alkyl groups to many electronegative groups under conditions present in cells. They stop tumor growth by cross-linking guanine bases in DNA double-helix strands - directly attacking DNA. This makes the strands unable to uncoil and separate. As this is necessary in DNA replication, the cells can no longer divide. In addition, these drugs add methyl or other alkyl groups onto molecules where they do not belong which in turn inhibits their correct utilization by base pairing and causes a miscoding of DNA. Alkylating agents are cell cycle-nonspecific. Alkylating agents work by three different mechanisms all of which achieve the same end result - disruption of DNA function and cell death. Mechanism Of Action Alkylating agents work by three different mechanisms: 1) attachment of alkyl groups to DNA bases, resulting in the DNA being fragmented by repair enzymes in their attempts to replace the alkylated bases, preventing DNA synthesis and RNA transcription from the affected DNA, 2) DNA damage via the formation of cross-links (bonds between atoms in the DNA) which prevents DNA from being separated for synthesis or transcription, and 3) the induction of mispairing of the nucleotides leading to mutations. Drug Category Antineoplastic Agents; ATC:L01AA03 Brand Names/Synonyms 3025 C. B.; ALKERAN; AT-290; Alkeran; CB 3025; L-PAM; L-Phenylalanine Mustard; L-Sarcolysin; L-Sarcolysine; L-Sarkolysin; Levofalan; Melfalan; Melphalan; Mephalan; NSC 8806; NSC-8806; Phenylalanine Mustard; Phenylalanine Nitrogen Mustard; Sarcolysine; Sarkolysin Dosage Forms tablets, injection Absorption incomplete, variable, 25-89% post oral dose Interactions DRUG INTERACTIONS There are no known drug/drug interactions with oral ALKERAN Vaccinations with live organism vaccines are not recommended in immunocompromised individuals Nalidixic acid together with high-dose intravenous melphalan has caused deaths in children due to haemorrhagic enterocolitis. Impaired renal function has been described in bone marrow transplant patients who were conditioned with high-dose intravenous melphalan and who subsequently received cyclosporin to prevent graft-versus-host disease Chemical IUPAC Name 2-amino-3-[4-[bis(2-chloroethyl)amino]phenyl]-propanoicacid Chemical Formula C13H18Cl2N2O2 Half Life 1.5 (+/-0.83) hours Drug Type Approved Drug # Accession No APRD00118 CAS Registry Number 148-82-3 |
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