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Phase I Study of SHR-A2102 in Patients With Advanced Solid Tumors

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ClinicalTrials.gov Identifier: NCT05701709
Recruitment Status : Not yet recruiting
First Posted : January 27, 2023
Last Update Posted : January 27, 2023
Information provided by (Responsible Party):
Shanghai Hengrui Pharmaceutical Co., Ltd.

Brief Summary:
The study was designed to evaluate the efficacy, safety, and pharmacokinetics of SHR2102 in patients with advanced solid tumors. The objective of this study was to determine the dose-limiting toxicity, maximum tolerance and recommended dose of SHR-A2102 in phase II study.

Condition or disease Intervention/treatment Phase
Advanced Solid Tumors Drug: SHR-A2102 Phase 1

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 200 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Intervention Model Description: SHR-A2102 single arm
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: An Open-Label, Single-Arm, Multi-Center Phase I Clinical Study to Evaluate the Safety, Tolerability, Efficacy and Pharmacokinetics of SHR-A2102 in Patients With Advanced Solid Tumors
Estimated Study Start Date : February 20, 2023
Estimated Primary Completion Date : August 31, 2025
Estimated Study Completion Date : August 31, 2025

Arm Intervention/treatment
Experimental: SHR-A2102 Drug: SHR-A2102
SHR-A2102 was given intravenously. Patients may continue to use SHR-A2102 until disease progression or unacceptable toxicity occurs.

Primary Outcome Measures :
  1. Number of participants with adverse events [ Time Frame: 24 months ]
    Adverse events are assessed by CTCAE v5.0

  2. Maximum tolerated dose (MTD) [ Time Frame: 12 weeks ]
    MTD is defined as the maximum dose within the first 3 weeks of multiple dosing that does not exceed the proportion of subjects who develop DLT as specified in the protocol's BOIN design.

  3. Recommended Phase 2 dose (RP2D) [ Time Frame: 24 months ]
    RP2D will be determined based on the available data for toxicity and PK.

  4. Dose Limiting Toxicity (DLT) [ Time Frame: 3 weeks ]
    Adverse events that occurred during the DLT observation period (the first period of study administration, a total of 21 days) that were determined to be related to the study drug (see protocol for details).

Secondary Outcome Measures :
  1. Peak plasma concentration (Cmax) [ Time Frame: 12 weeks ]
  2. Area under the plasma concentration versus time curve (AUC) [ Time Frame: 12 weeks ]
  3. T1/2 (Half-life) [ Time Frame: 12 weeks ]
    The time required for the plasma concentration of a drug to be reduced by 50%

  4. Immunogenicity: Number of subjects with anti-SHR-A2102 antibody (ADA), incidence, occurrence time, duration, etc [ Time Frame: 12 weeks ]
  5. Objective response rate (ORR) [ Time Frame: 24 months ]
  6. duration of response (DoR) [ Time Frame: 24 months ]
  7. disease control rate (DCR) [ Time Frame: 24 months ]
  8. progression-free survival (PFS) [ Time Frame: 24 months ]
  9. overall survival (OS) [ Time Frame: 24 months ]

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  1. Able and willing to provide a written informed consent;
  2. Age ≥18 years old, gender unlimited;
  3. The physical status score of the Eastern Tumor Cooperative Group (ECOG) was 0 ~ 1;
  4. Life expectancy Predicted survival ≥3 months;
  5. Histologically or cytologically confirmed advanced or metastatic malignant tumor; Patients with advanced solid tumors confirmed by pathology who have failed or been intolerant to standard treatment, have no standard treatment or refuse standard treatment;
  6. There is at least one measurable lesion that meets the RECIST 1.1 criteria.

Exclusion Criteria:

  1. Plan to receive any other antitumor therapy during this trial;
  2. Receiving other investigational drugs or treatments that are not on the market within 4 weeks prior to the initial administration of the study drug;
  3. Received antitumor therapy such as chemotherapy, radiotherapy, biotherapy, targeted therapy, or immunotherapy within 4 weeks prior to first administration of the study drug (nitrosourea or mitomycin C within 6 weeks prior to first administration; Oral fluorouracil within 2 weeks prior to initial first administration); Palliative radiotherapy or local therapy within 2 weeks before first administration use of the study drug;
  4. Had major surgery other than diagnosis or biopsy within 4 weeks prior to the study's initial dosing;
  5. Treatment with CYP3A4, CYP2D6, P-gp or BCRP booster or inducer is less than 5 drug half-life from the date of first administration;
  6. According to NCI-CTCAE v5.0, adverse events caused by previous antitumor therapy did not recover to ≤ grade 1 (except hair loss; In the judgment of the investigator, after consultation with the sponsor, some tolerable chronic grade 2 toxicity may be excluded);
  7. Inadequately treated central nervous system (CNS) metastases, or the presence of uncontrolled or symptomatic active CNS metastases, may be characterized by the presence of clinical symptoms, cerebral edema, spinal cord compression, cancerous meningitis, pia meningeal disease, and/or rapid progression. Patients with CNS metastases that have been adequately treated and whose neurological symptoms return to baseline at least 4 weeks prior to randomization (except for residual signs or symptoms associated with CNS treatment) may be enrolled. In addition, subjects must either stop corticosteroids or receive prednisone (or an equivalent dose of another corticosteroid) at least 4 weeks prior to randomization;
  8. Any other malignancies, excluding cured basal cell carcinoma of the skin and carcinoma in situ of the cervix, etc. within 5 years prior to initial administration;
  9. A history of clinically significant lung disease (such as interstitial pneumonia, radiation pneumonia, pulmonary fibrosis) or chest imaging during screening suggests any such disease;
  10. Severe infections that require intravenous antibiotic, antiviral or antifungal control;
  11. Active HBV or HCV infection (HBsAg positive and viral copy number ≥2000 IU/mL, HCV antibody positive and HCV RNA higher than the lower limit of detection method);
  12. History of immunodeficiency (including HIV positive, other acquired or congenital immunodeficiency diseases) or organ transplantation;
  13. Concomitant diseases (such as severe diabetes, thyroid disease, and psychosis) or any other conditions that, in the investigator's judgment, seriously endanger the patient's safety or affect the patient's ability to complete the study.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT05701709

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Contact: Fei Luo +0518-81220121 fei.luo@hengrui.com

Sponsors and Collaborators
Shanghai Hengrui Pharmaceutical Co., Ltd.
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Responsible Party: Shanghai Hengrui Pharmaceutical Co., Ltd.
ClinicalTrials.gov Identifier: NCT05701709    
Other Study ID Numbers: SHR-A2102-I-102
First Posted: January 27, 2023    Key Record Dates
Last Update Posted: January 27, 2023
Last Verified: January 2023
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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