A double-blind, placebo-controlled, efficacy, safety, and pharmacokinetic study of INN 00835, a novel antidepressant peptide, in the treatment of major depression

被引:17
作者
Feighner, JP
Ehrensing, RH
Kastin, AJ
Leonard, BE
Sverdlov, L
Nicolau, G [1 ]
Patel, A
Hlavka, J
Abajian, H
Noble, JF
机构
[1] Innapharma Inc, Suffern, NY 10901 USA
[2] Feighner Res Inst, San Diego, CA USA
[3] Ochsner Clin & Alton Ochsner Med Fdn, New Orleans, LA USA
[4] VA Med Ctr, New Orleans, LA USA
[5] Tulane Univ, Sch Med, New Orleans, LA 70112 USA
[6] Natl Univ Ireland Univ Coll Galway, Galway, Ireland
关键词
antidepressants; peptides; serotonin;
D O I
10.1016/S0165-0327(99)00187-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: INN 00835 is a synthetic pentapeptide with a potential for rapid onset of action as an antidepressant. Its efficacy was investigated in a pilot study in patients diagnosed with major depression. Methods: Fifty two patients received either active drug - INN 00835 (26 patients) - or placebo (26 patients), subcutaneously at 0.2 mg/kg for 5 consecutive days. The patients were evaluated for an additional 4 weeks after treatment. Efficacy was evaluated by the following psychiatric rating scales: HAMD, MADRS, CSRS, CGI, and VAS. The effect of treatment was also evaluated by using a biochemical marker: changes in blood platelet serotonin (5HT) uptake rates in drug-treated patients compared to those in the placebo group. Plasma concentrations of INN 00835 were measured by LC/MS. Results: Statistical analysis indicated a strong pharmacodynamic correlation between plasma drug concentrations at 1 h after dosing and the reduction in the severity of depression as measured by the psychiatric rating scales. A minimum effective plasma concentration (MEC) of INN 00835 was 5 ng/ml. Statistically significant differences in response to treatment (P < 0.05) were found between patients with plasma concentrations above MEC and those in the placebo group, as well as between subjects with plasma concentrations above and below the MEG. The peak effect was observed after the 5-day treatment and the response to treatment persisted during the 4-week follow-up period. The change of 5HT uptake rates after treatment was significantly larger in the drug-treated group than in the placebo group. Limitations: This was a pilot study conducted in a relatively small population (52 patients) and the limited number of blood sampling times did not allow a comprehensive pharmacokinetic analysis. There was a relatively large placebo response. The results have to be confirmed in future, large scale studies. Conclusions: INN 00835 appears to be a promising drug for the treatment of major depression. (C) 2000 Elsevier Science B.V. All rights reserved.
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页码:119 / 126
页数:8
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