Abstract | BACKGROUND: METHODS: We evaluated coadministered trimethobenzamide with apomorphine in 182 PD subjects using a randomized, double-blind, placebo-controlled design, with phased withdrawal of subjects from trimethobenzamide to placebo. Evaluations included presence/absence of nausea and vomiting; Index of Nausea, Vomiting, and Retching (INVR); subject evaluation of medication; Unified Parkinson's Disease Rating Scale (UPDRS) motor score; "on" response post-injection; and safety assessments. RESULTS: Incidence of nausea and/or vomiting on Day 1 of apomorphine initiation (primary endpoint) was not significantly different between trimethobenzamide and placebo. Over a longer period, a significantly lower incidence was found for trimethobenzamide during Period 1 (Days 1-28, p = 0.025) and Period 2 (Days 29-56, p = 0.005), with no difference during Period 3 (Days 57-84). INVR results were generally more favorable with trimethobenzamide than placebo in Period 1 and significantly more favorable in Period 2. The majority of subjects in both groups achieved an "on" response after apomorphine injection at all assessments. No significant differences were found between groups for UPDRS motor scores. No added safety risk with concomitant use of trimethobenzamide and apomorphine was found. CONCLUSION:
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Authors | Robert A Hauser, Stuart Isaacson, Thomas Clinch, Tigan/Apokyn Study Investigators |
Journal | Parkinsonism & related disorders
(Parkinsonism Relat Disord)
Vol. 20
Issue 11
Pg. 1171-6
(Nov 2014)
ISSN: 1873-5126 [Electronic] England |
PMID | 25239603
(Publication Type: Clinical Trial, Phase IV, Journal Article, Randomized Controlled Trial)
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Copyright | Copyright © 2014 Elsevier Ltd. All rights reserved. |
Chemical References |
- Antiemetics
- Benzamides
- Dopamine Agonists
- Apomorphine
- trimethobenzamide
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Topics |
- Adult
- Aged
- Aged, 80 and over
- Analysis of Variance
- Antiemetics
(therapeutic use)
- Apomorphine
(adverse effects, therapeutic use)
- Benzamides
(therapeutic use)
- Dopamine Agonists
(adverse effects)
- Double-Blind Method
- Female
- Follow-Up Studies
- Humans
- Injections, Subcutaneous
(adverse effects)
- Male
- Middle Aged
- Nausea
(chemically induced, drug therapy)
- Parkinson Disease
(drug therapy)
- Severity of Illness Index
- Time Factors
- Vomiting
(chemically induced, drug therapy)
- Young Adult
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