Skip to content

Study of safety and efficacy of DKY709 alone or in combination with PDR001 in patients with advanced solid tumors.

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-513281-19-00
Acronym
CDKY709A12101C
Enrollment
32
Registered
2024-08-08
Start date
2024-11-25
Completion date
Unknown
Last updated
2025-06-04

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

Conditions

Cutaneous Melanoma, Microsatellite Stable Colorectal Cancer, Nasopharyngeal Carcinoma, Non-Small Cell Lung Cancer, Triple Negative Breast Cancer

Interventions

None listed

Sponsors

Novartis Pharma AG
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Countries

Germany, Spain

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026