Recruiting
Study of DM5167 in Patients With Advanced Solid Tumors
DM5167 is a second-generation of PARP inhibitor that selectively targets the PARP-1 enzyme. This results in less haematological toxicity and a high level of safety. The aim of the study is to assess the safety and tolerability of DM5167 in patients with advanced solid tumors not respond to other treatments.
ClinicalTrials.gov IDNCT07101601
PhasePHASE1
Enrollment58
SponsorDIGMBIO
Age19 Years
SexALL
Conditions studied
Advanced Breast Cancer
About this study
DM5167 is a second-generation of PARP inhibitor that selectively targets the PARP-1 enzyme. This results in less haematological toxicity and a high level of safety. The aim of the study is to assess the safety and tolerability of DM5167 in patients with advanced solid tumors not respond to other treatments.
Interventions
- Drug: DM5167 — Once daily for 28 days
Primary outcomes
- Part 1: Incidence of dose limiting toxicities (DLT) of DM5167 (During the first cycle (28 days) of DM5167 treatment)
- Part 1 and Part 2: Treatment emergent adverse events (TEAE) and serious adverse events (SAEs) (First dose up to 28 days post end of treatment)
Eligibility information
Inclusion Criteria:
* Men and women aged 19 years or older as of the date of written informed consent
* Patients who have at least one measurable lesion according to RECIST version 1.1
* ECOG performance status ≤ 1
* Patients with life expectancy ≥ 12 weeks
* Patients who meet the clinical laboratory test criteria confirming adequate liver, renal, and hematologic function
* Patients who voluntarily provide written informed consent to participate in this study
* Patients with histologically or cytologically confirmed unresectable advanced solid tumors
* Patients who have BRCA1/BRCA2 mutations
Exclusion Criteria:
* Patients with a medical history of significant illness
* Patients with QT interval of \> 450 ms (for men) or \> 460 ms (for women)\\
* Patients who have not yet recovered from toxicity related to previous anticancer therapy
* Patients were predicted to demonstrate hypersensitivity to the components of the investigational medicinal product
* Patients who have participated in another clinical trial and received an investigational product or medical device
* Other individuals deemed inappropriate for participation in the study by the investigator
Study locations
- Seoul National University Bundang Hospital, Gyeonggi-do, South Korea
- Samsung Medical Center, Seoul, South Korea
- Seoul National University Hospital, Seoul, South Korea
- Severance Hospital, Seoul, South Korea
Before you participate: Varda Clinical is an independent discovery tool, not the study sponsor or a medical provider. Eligibility can only be determined by the official study team. Discuss potential risks and benefits with a qualified healthcare professional.
Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-09-30.