Not yet recruiting NCT07567859
A Study of HS-10587 in Patients With Advanced Solid Tumors
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: HS-10587.
- Who it may be relevant to
- Registry conditions: MTAP Deletion. Basic parameters: 18 years — 75 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
An Open-Label, Multi-Center Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic/Pharmacodynamic Characteristics, and Preliminary Efficacy of HS-10587 in Patients With Methylthioadenosine Phosphorylase (MTAP)-Deleted Advanced Solid Tumors
Overview
This is a Phase I, multicenter, open-label clinical trial with dose escalation/dose expansion phases, designed to evaluate the safety, tolerability, pharmacokinetic/pharmacodynamic (PK/PD) profiles, and antitumor efficacy characteristics of HS-10587 in patients with MTAP-deleted advanced solid tumors.
Interventions
- Drug HS-10587
HS-10587 tablet
Primary outcome measures
- Incidence of DLT [Time frame: Up to 21 days after the first administration. (first cycle)]
- MTD or MAD [Time frame: Up to 21 days after the first administration. (first cycle)]
Secondary outcome measures (11)
- Incidence of adverse events (AEs) and serious adverse events (SAEs) [Time frame: From time of informed consent to 28 days post last dose of HS-10587.]
- Pharmacokinetics (PK) profile of HS-10587 in patients with advanced solid tumors [Time frame: Predose and postdose up to end of treatment, approximately 2 years]
- Pharmacokinetics (PK) profile of HS-10587 in patients with advanced solid tumors [Time frame: Predose and postdose up to end of treatment, approximately 2 years.]
- Pharmacokinetics (PK) profile of HS-10587 in patients with advanced solid tumors [Time frame: Predose and postdose up to end of treatment, approximately 2 years.]
- Pharmacokinetics (PK) profile of HS-10587 in patients with advanced solid tumors [Time frame: Predose and postdose up to end of treatment, approximately 2 years]
- Efficacy of HS-10587 in patients with advanced solid tumors [Time frame: Predose and post dose up to end of treatment, approximately 2 years]
- Efficacy of HS-10587 in patients with advanced solid tumors. [Time frame: Predose and post dose up to end of treatment, approximately 2 years.]
- Efficacy of HS-10587 in patients with advanced solid tumors. [Time frame: Predose and post dose up to end of treatment, approximately 2 years]
- Efficacy of HS-10587 in patients with advanced solid tumors. [Time frame: Predose and post dose up to end of treatment, approximately 2 years.]
- Efficacy of HS-10587 in patients with advanced solid tumors. [Time frame: Predose and post dose up to end of treatment, approximately 2 years.]
- Efficacy of HS-10587 in patients with advanced solid tumors. [Time frame: Predose and post dose up to end of treatment, approximately 2 years]
Eligibility criteria
Inclusion criteria
- Participants who voluntarily participate in this clinical study, understand the study procedures, and are able to sign a written ICF.
- Participants with locally advanced or recurrent metastatic malignant solid tumors confirmed by histopathology or cytopathology who have failed or are intolerant to at least one line of prior standard treatment, or for whom no standard treatment exists.
- Evidence of MTAP deletion in the tumor tissue.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
- Life expectancy ≥12 weeks.
- At least one measurable lesion that would qualify as target lesion by Response Evaluation Criteria in Solid Tumors, Version 1.1 (RECIST 1.1).
- Female participants of childbearing potential are willing to take appropriate contraceptive measures and should not breastfeed; male participants are willing to use barrier contraception.
Exclusion criteria
- History of other primary malignancies.
- Presence of pleural/abdominal effusion or pericardial effusion requiring clinical intervention.
- Presence of leptomeningeal metastasis, spinal cord compression, or brainstem metastasis; known untreated brain metastases, or symptomatic/unstable brain metastases.
- Participants who have any Grade ≥ 2 residual toxicity according to Common Terminology Criteria for Adverse Events (CTCAE, version 6.0) from prior anti-tumor therapies (except alopecia, pigmentation, and residual neurotoxicity).
- Inadequate bone marrow reserve or hepatic and renal functions.
- Severe, uncontrolled, or active cardiovascular diseases.
- Severe or poorly controlled diabetes.
- Severe or poorly controlled hypertension.
- Severe infection within 4 weeks prior to the first dose.
- Long-term corticosteroid therapy, history of other acquired/congenital immunodeficiency disorders, or organ transplantation.
- Known active infectious diseases.
- Clinically significant gastrointestinal dysfunction.
- Moderate to severe pulmonary diseases that seriously affect respiratory function.
- Prior history of severe neurological or mental disorders.
- Female participants who are pregnant or breastfeeding, or plan to become pregnant during the study.
- History of severe allergies, or history of hypersensitivity reactions to any active or inactive ingredients of HS-10587 or to drugs with similar chemical structures to HS-10587 or drugs of the same class as HS-10587.
- Participants with any conditions that may jeopardize participant safety or interfere with study assessments, as judged by the investigator.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07567859 · HS-10587-101