Relistor approved for OIC
PHARMACOLOGIC CLASS: Opioid antagonist (peripheral)
ACTIVE INGREDIENT: Methylnaltrexone bromide 12mg/0.6mL; soln for SC inj.
INDICATION: Opioid-induced constipation.
PHARMACOLOGY: The use of opioid analgesics can lead to constipation due to their effect on intestinal smooth muscle and their interference with normal bowel elimination function. Methylnaltrexone bromide is a mu-opioid receptor antagonist that has limited ability to cross the blood-brain barrier. It blocks the effects of opioids in peripheral tissues, including the GI tract, mitigating their constipating effects without interfering with their centrally-mediated analgesia.
CLINICAL TRIALS: The results of 2 placebo-controlled studies demonstrated the efficacy and safety of Relistor in treating opioid-induced constipation. The studies involved 287 patients with advanced illness (eg, incurable cancer, endstage COPD, heart failure, Alzheimer's disease, AIDS). Before screening, patients had been receiving palliative opioid therapy and had opioid-induced constipation. They were on a stable opioid regimen for at least 3 days before randomization. The first study compared single doses of the study drug (0.15mg/kg or 0.3mg/kg) to placebo in a double-blind phase that was followed by an open-label 4-week period in which Relistor was used as needed. The primary endpoint was the proportion of patients with rescue-free laxation within 4 hours of the double-blind dose of the study drug. Patients given either dose of Relistor had a significantly higher rate of laxation than those given placebo. In the second trial, either the study drug or placebo was given every other day for 2 weeks. During the first week, patients received either Relistor 0.15mg/kg or placebo. In the second week, the dose could be increased to 0.3mg/kg if needed (≤2 rescue-free laxations up to day 8). Patients given the study drug had a higher rate of laxation within 4 hours of the first dose than those given placebo, and they had significantly higher rates of laxation within 4 hours after at least 2 of the first 4 doses. The laxation response rate was shown to be consistent from the first dose to the 7th dose over the 2-week period. There was no relationship seen between baseline opioid doses and the laxation response in patients given Relistor. Daily opioid use did not change substantially in either the patients given the study drug or those given placebo, and there was no relevant changes in pain scores from baseline between the groups. Open-label extension studies indicate that the drug maintains its effectiveness for up to 4 months of treatment.
ADULTS: Give by SC inj in upper arm, abdomen, or thigh once every other day as needed (max 1 dose/24hrs); rotate inj sites. <38kg or >114kg: 0.15mg/kg. 38–<62kg: 8mg. 62–114kg: 12mg. Severe renal impairment (CrCl<30mL/min): reduce dose by 1/2.
CHILDREN: Not recommended.
CONTRAINDICATIONS: Mechanical GI obstruction (known or suspected).
PRECAUTIONS: Re-evaluate if severe or persistent diarrhea occurs. Peritoneal catheterization. Bowel movement may occur within 30min of dosing. Pregnancy (Cat.B). Nursing mothers.
ADVERSE REACTIONS: Abdominal pain, flatulence, nausea, dizziness, diarrhea.
HOW SUPPLIED: Single-use vial—1 Kit (w. 7 vials, syringes, needles, supplies)— 1
For more information call (800) 934-5556 or visit www.Relistor.com