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A Phase 2 to Evaluate the Dose-Response Relationship and Safety of JTT-751 in Patients with Iron Deficiency Anemia

A Phase 2 to Evaluate the Dose-Response Relationship and Safety of JTT-751 in Patients with Iron Deficiency Anemia

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2080223256
Enrollment
120
Registered
2016-07-06
Start date
2016-07-04
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

Iron deficiency anemia

Interventions

Sponsors

Japan Tobacco Inc.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Iron deficiency anemia Hemoglobin level of= > 7.0 g/dL and < 11.0 g/dL

Exclusion criteria

Exclusion criteria: Anemia caused by other than iron deficiency Serum phosphate < 2.5 mg/dL Uncontrollable treatment potentially affecting bleeding in patients with bleeding lesion

Design outcomes

Primary

MeasureTime frame
efficacy Changes in hemoglobin level

Secondary

MeasureTime frame
efficacy Changes in erythrocyte- and iron-related test values

Countries

Japan

Outcome results

None listed

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