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Open clinical trial of Leuprorelin Acetate (SR) in patients with Kennedy-Alter-Sung syndrome (KAS)

Open clinical trial of Leuprorelin Acetate (SR) in patients with Kennedy-Alter-Sung syndrome (KAS) - Open clinical trial of Leuprorelin Acetate (SR) in patients with KAS

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000001455
Enrollment
10
Registered
2008-10-23
Start date
2008-10-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Kennedy-Alter-Sung syndrome (KAS)

Interventions

Leuprorelin acetate (SR) 11.25mg subcutaneous infection per 12 weeks

Sponsors

Department of Neurology Chiba University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Genetically confirmed KAS patients with written informed concent, who have no desire to father achild, no severe disturbance in liver and renal functions, and can stand for 6 min.

Exclusion criteria

Exclusion criteria: "1) Patients who have taken any drugs which effect serum teststerone level within 48 weeks prior to the informed consent. 2) Patients who have taken any drugs which rduce serum teststerone level for more than 48 weaks prior to the informed concent. 3) Patients who have undergone surgical castration. 4) Patients with major depression. 5) Patients who have severe complications including sereve hypertention. 6) Patients who cannot undergo the clinical tests included in this trial. 7) Patients with allergy to leuprorelin acetate.

Design outcomes

Primary

MeasureTime frame
Pharyngeal barium residue in videofluorography

Secondary

MeasureTime frame
serum CK, parameters in videofluorography, frequency of 1C2 antibody staining in scrotal skin, clinical scores, clinical scores, QOL scores, parameters in electrophysiological testings

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026