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39-301: Special Drug Use-Results Survey of DEMSER

39-301: Special Drug Use-Results Survey of DEMSER (Improvement of catecholamine hypersecretion in pheochromocytoma)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT2031240474
Enrollment
250
Registered
2024-11-08
Start date
2019-06-11
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

Pheochromocytoma

Interventions

None listed

Sponsors

Nakao Takafumi
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who have recieved DEMSER for improvement of catecholamine hypersecretion in pheochromocytoma

Exclusion criteria

Exclusion criteria: none

Design outcomes

Primary

MeasureTime frame
Safety items : Occurrence of adverse drug reactions and infections, factors considered to influence the safety Efficacy items : Overall improvement, metanephrines fractionation (24-hour urine collection, spot urine, free), catecholamines 3 fractionation (24-hour urine collection, spot urine, plasma), factors considered to influence the efficacy

Contacts

Public ContactTakafumi Nakao

Ono Pharmaceutical Co.,LTD

pms_contact_ml@ono-pharma.com+81-6-6222-5501

Outcome results

None listed

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