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Rekambys Drug Use Results Survey

Rekambys Drug Use Results Survey - Rekambys Drug Use Results Survey

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000051600
Enrollment
140
Registered
2023-07-15
Start date
2022-11-09
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

HIV/AIDS

Interventions

None listed

Sponsors

Janssen Pharmaceutical K.K.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with HIV infection who administrated Rekambys

Exclusion criteria

Exclusion criteria: NA

Design outcomes

Primary

MeasureTime frame
Safety (ADR) Effectiveness(Changes in HIV-RNA level, Changes in CD4 lymphocyte count)

Countries

Japan

Contacts

Public ContactKazuyo Izumiya

Post-approval Delivary Unit Janssen Pharmaceutical K.K. Post-approval Delivary Unit

kizumiya@its.jnj.com03-4411-5031

Outcome results

None listed

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