Reversal of Antipsychotic-Induced Hyperprolactinemia, Weight Gain, Hyperglycemia and Dyslipidemia

Phase 4

• Conditions: Hyperprolactinemia; Weight Gain; Dyslipidemia

• Registration Number: NCT00541554
• Lead Sponsor: Genovate Biotechnology Co., Ltd.,

Brief Summary

This is a prospective, open-label study to evaluate the efficacy and safety in reducing antipsychotic-induced hyperprolactinemia, weight gain, and dyslipidemia by aripiprazole. Approximate 60 patients will be recruited to achieve at least 40 evaluable patients.

Detailed Description

A.Screening / Baseline visit (V1; Day 0) After signing the informed consent form, patients' DSM-IV multiaxial examination, physical examination, vital sign, pregnancy test, BMI will be conducted. The demographics, medical history, and concomitant medication will be recorded. After evaluating all variables obtained, the eligible patients will be enrolled into study.Patients who fulfill the inclusion / exclusion criteria will be performed the laboratory tests, PANSS, EPS (AIMS \& BARS), menstrual function, sexual function (Arizona sexual experience scale) and prolaction. Afterwards, the treatment period will be started to add-on with first medication (7.5 or 15 mg daily by patient, which was prescribed by investigator) to current antipsychotics at this visit. Besides, drug accounting and adverse events will also be recorded at this visit. Patients are maintained on current doses of antipsychotics, and all other medicines.

B.Treatment phase (V2\~V3; 2\~4 Week finished; 14±3\~28±3 Day finished) The vital sign, physical examination, BMI, laboratory tests (at V3), PANSS, EPS (AIMS \& BARS), menstrual function, sexual function (Arizona sexual experience scale), and prolactin will be carried out. Concomitant medication, adverse events, and drug accounting will also be recorded at this visit. Study drug could be titrated with a flexible dose from 7.5 to 30 mg QD. All dose adjustments should be made with the approval of the investigator.

C.Completion visit (V4; 8 Week Finished; 56±7 Day finished, or Early termination) The vital sign, physical examination, pregnancy test, BMI, laboratory tests, PANSS, EPS (AIMS \& BARS), menstrual function, sexual function (Arizona sexual experience scale), prolactin will be carried out. Concomitant medication, adverse events, and drug accounting will also be recorded at this visit.

Study Timeline

• Status Verified: 2007-10
• Study Start: 2007-10
• Study First Submitted: 2007-10-08
• Study First Submitted QC: 2007-10-09
• Last Update Submitted: 2007-10-09
• Study First Posted: 2007-10-10
• Last Update Posted: 2007-10-10
• Study Completion: 2009-02

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

1. Male or female in age between 12 and 65 years old.
2. Clinical diagnosis of schizophrenia, schizoaffective disorder, or bipolar disorder with DSM-IV criteria.
3. Keep stable dosage of the same antipsychotic other than aripiprazole during last one month.
4. Who are currently taking antipsychotic drugs and for whom an alteration in medication is clinically reasonable. This includes patients who are stable or who have symptoms that are not optimally controlled or patients experiencing tolerability problems.
5. Having antipsychotic-induced symptomatic hyperprolactinemia, weight gain, increased plasma glucose or dyslipidemia judged by the investigator.
6. Informed Consent was obtained from the subject and legal guardian (if necessary).

Exclusion Criteria

1. Pregnant or breast feeding women or planning a pregnancy.
2. Patient has a history of hypersensitivity or allergy to investigated drug.
3. Acute psychosis, acute suicidal ideation, or any acute psychiatric condition that might require emergent intervention.
4. Any clinical condition or significant concurrent disease judged by the investigator to complicate the evaluation of the study treatment.
5. Having participated other investigational drug study and taken the investigation drug within one month prior to study entry.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP