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A Phase 1 Study of LY3039478 in Japanese Patients with Advanced Solid Tumors I6F-JE-JJCC

A Phase 1 Study of LY3039478 in Japanese Patients with Advanced Solid Tumors I6F-JE-JJCC

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2080223309
Enrollment
Unknown
Registered
2016-09-01
Start date
2016-09-01
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

Advanced Solid Tumor

Interventions

investigational material(s) Generic name etc : LY3039478 INN of investigational material : Therapeutic category code : 429 Other antitumor agents Dosage and Administration for Investigational materia

Sponsors

Eli Lilly Japan K.K.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: -Histological or cytological evidence of a diagnosis of solid tumor that is advanced and/or metastatic. -In the judgment of the investigator, participants must be appropriate candidates for experimental therapy after available standard therapies have failed or for whom standard therapy is not appropriate. -Performance status of less than or equal to 1 on the Eastern Cooperative Oncology Group (ECOG) scale. -Adequate organ function, including hematologic, hepatic, and renal. -Estimated life expectancy of more than or equal to 12 weeks.

Exclusion criteria

Exclusion criteria: -Received previous therapy for cancer within 14 or 21 days of the initial dose of study drug for a nonmyelosuppressive or myelosuppressive agents, respectively. -Have serious preexisting medical conditions. -Have current or recent (within 3 months of study drug administration) gastrointestinal disease with chronic or intermittent diarrhea. -Have an active bacterial, fungal, and/or known viral infection. -Have known acute or chronic leukemia or current hematologic malignancies that may affect the interpretation of results.

Outcome results

None listed

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