A Study of HDM2005 in Patients With Advanced Solid Tumor

Official title

A Phase Ia/Ib Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Antitumor Activity of HDM2005 in Patients With Advanced Solid Tumors

Overview

This is a study evaluating the efficacy, safety, and pharmacokinetics ofHDM2005 in participants with metastatic solid tumors.

Interventions

• Drug HDM2005
  HDM2005 will be administered via IV infusion.

Primary outcome measures

• Incidence of dose limiting toxicity (DLT) events (for dose escalation phase) [Time frame: up to 21 days or 28 days following first dose]
• Incident and severity of adverse events(for dose escalation phase) [Time frame: Until 28 days after the last dose or initiation of a new antineoplastic therapy, whichever occurs first.]
• Progression-free survival(PFS)(for dose expansion phase) [Time frame: Approximately 30 months]
• Objective Response Rate (ORR)(for dose expansion phase) [Time frame: Approximately 18 months]
• Recommended Phase 2 Dose (RP2D) (for dose expansion phase) Recommended Phase 2 Dose (RP2D) (for dose expansion phase) Recommended Phase 2 Dose (RP2D) (for dose expansion phase) [Time frame: Approximately 30 months]

Secondary outcome measures (6)

• Plasma concentration of HDM2005, total antibody and the free MMAE [Time frame: up to 28 days following last dose]
• Immunogenicity [Time frame: up to 28 days following last dose]
• Objective Response Rate (ORR)(for dose escalation phase) [Time frame: Approximately 18 months]
• Time to Response (TTR) [Time frame: Approximately 30 months]
• Duration of Response (DOR) [Time frame: Approximately 30 months]
• Overall survival (OS) [Time frame: Approximately 30 months]

Eligibility criteria

Inclusion criteria

• Agree to follow the study treatment protocol and visit schedule, enroll voluntarily and sign a written informed consent.
• Male or female aged ≥ 18 years at the time of signing the ICF;
• ECOG performance status of 0-1.
• Life expectancy of at least 3 months.
• Specific types of advanced solid tumors that have been confirmed by histopathological examination.
• Has metastatic disease that has progressed during or following previous treatment appropriate for the disease type.
• All subjects are required to provide archived tissue (5 unstained sections) obtained within the previous 2 years or fresh tissue for ROR1 expression testing at the central laboratory.
• Presence of radiographically measurable disease.
• Subjects must have recovered (to ≤ Grade 1) from any AE associated with prior anticancer therapy.
• Has adequate organ function.
• Female subjects of childbearing potential should agree to use contraception methods during the study and for 6 months after the end of the study; have a negative serum pregnancy test within 7 days before study enrollment; and male subjects should agree to use contraceptive avoidance measures during the study and for 6 months after the end of the study.

Exclusion criteria

• Patients with active brain metastases (defined as stable for < 4 weeks, or symptomatic, or requiring antiepileptic drug/hormonal therapy, or meningeal metastases).
• Subjects have another primary malignancy ,with the following exceptions: adequately treated non-melanoma skin cancer without evidence of disease recurrence and adequately treated carcinoma in situ without evidence of disease recurrence,et al.
• History of severe bleeding disorders .
• History of chronic pancreatitis or acute pancreatitis within 6 months.
• History of interstitial lung disease, radiation pneumonitis requiring steroid therapy, or any evidence of clinically active interstitial lung disease.
• Patients with uncontrolled pleural effusion, pericardial effusion or ascites requiring repeated drainage after intubation and drainage,VEGF inhibitors, platinum and other drugs injection (subjects with stable symptoms for at least one week after treatment can be enrolled).
• Prior solid organ transplantation.
• Has peripheral neuropathy of Grade >1.
• Has significant cardiovascular or cerebrovascular diseases.
• Has an uncontrolled ongoing infection.
• Active infectious disease, such as HIV infection, active hepatitis B, active hepatitis C (positive RNA result), active syphilis.
• Receiving corticosteroids (prednisone equivalent more than10 mg/day).
• Contraindication to any component of HDM2005.
• History of drug anaphylactic shock, severe food allergy, uncontrolled asthma or COPD.
• Female subjects who are pregnant, lactating or planning to become pregnant during the study.
• Known history of mental illness or substance abuse that would impair the subject's ability to cooperate with study requirements.
• Prior or current evidence of any disease, treatment, or laboratory abnormality that, in the opinion of the investigator, could affect the outcome of the study, prevent the subject from participating in the study entirely, or is not in the subjects' best interest.

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

Sequential

Masking

Open label

Primary purpose

Treatment

Study locations

China · 1 center

• Fudan University shanghai Cancer Center — Shanghai

Identifiers

NCT: NCT07004296 · HDM2005-103

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗