A Study of ICP-033 in Patients With Advanced Solid Tumors

February 5, 2024 updated by: Beijing InnoCare Pharma Tech Co., Ltd.

A Phase I Clinical Trial to Evaluate the Safety, Tolerability, and Pharmacokinetics of ICP-033 in Patients With Solid Tumors

A Dose finding Study to Evaluate the Safety, Tolerability and Pharmacokinetics and Preliminary Anti-Tumor Activity of ICP-033 Tablets in Patients with Advanced Solid Tumors.

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Recruiting

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Interventional

Enrollment (Estimated)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
60

Phase

Phase

The stage of a clinical trial studying a drug or biological product, based on definitions developed by the U.S. Food and Drug Administration (FDA). The phase is based on the study's objective, the number of participants, and other characteristics. There are five phases: Early Phase 1 (formerly listed as Phase 0), Phase 1, Phase 2, Phase 3, and Phase 4. Not Applicable is used to describe trials without FDA-defined phases, including trials of devices or behavioral interventions.
  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact

The name and contact information for the person who can answer enrollment questions for a clinical study. Each location where the study is being conducted may also have a specific contact, who may be better able to answer those questions.

Study Locations

  • China
    • Chengdu
      • Sichuan, Chengdu, China, 610041
        • Recruiting
        • West China Hospital of Sichuan University
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

18 years to 75 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  1. Eastern Cooperative Oncology Group (ECOG) performance status of 0-1;
  2. Patients with histologically confirmed locally advanced unresectable or metastatic solid tumors;
  3. At least one measurable lesion according to RECIST 1.1.

Exclusion Criteria:

  1. Pregnant and lactating women, or women planning to become pregnant during the study through at least 6 months after the last dose of study drug.
  2. Patients with unstable primary central nervous system (CNS) tumors or CNS metastases.
  3. Patients who have active or history of interstitial lung disease or noninfectious pneumonia.
  4. Patients with QTc > 450 ms in males and > 470 ms in females on ECG at screening, or other clinically significant abnormalities in the ECG at the discretion of the investigator.
  5. Patient with the Medication history and surgical history as stated in the protocol
  6. Those who are unsuitable for blood collection or contraindicated for blood collection.
  7. Other conditions considered unsuitable for participation in this trial at the discretion of the investigator.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm

Participant Group / Arm

A group or subgroup of participants in a clinical trial that receives a specific intervention/treatment, or no intervention, according to the trial's protocol.
Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.
Experimental: ICP-033 Dose Escalation
Drug: ICP-033 tablet Administered orally，once a day，every 28 days is a cycle.
Drug: ICP-033 tablet
Administered orally, once a day, 28 days per cycle

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Measure Description
Time Frame
The incidence and severity of adverse event (AE) of ICP-033 assessed by NCI-CTCAE V5.0.
Time Frame: through study completion, an average of 2 years
To assess the safety and tolerability of ICP-033 in patients with advanced solid tumors.
through study completion, an average of 2 years
Dose-Limiting Toxicities (DLTs)
Time Frame: through study completion, an average of 2 years
To assess the safety and tolerability of ICP-033 in patients with advanced solid tumors.
through study completion, an average of 2 years
Maximum tolerated dose (MTD)
Time Frame: through study completion, an average of 2 years
To assess the safety and tolerability of ICP-033 in patients with advanced solid tumors.
through study completion, an average of 2 years
Recommended phase II dose (RP2D)
Time Frame: through study completion, an average of 2 years
through study completion, an average of 2 years

Secondary Outcome Measures

Secondary Outcome Measures

In a clinical study's protocol, a planned outcome measure that is not as important as the primary outcome measure for evaluating the effect of an intervention but is still of interest. Most clinical studies have more than one secondary outcome measure.
Outcome Measure
Measure Description
Time Frame
The maximum plasma concentration observed (Cmax)
Time Frame: through study completion, an average of 2 years
To evaluate the pharmacokinetic (PK) characteristics of ICP-033 in patients with solid tumors.
through study completion, an average of 2 years
Time of maximum observed plasma concentration (Tmax)
Time Frame: through study completion, an average of 2 years
To evaluate the pharmacokinetic (PK) characteristics of ICP-033 in patients with solid tumors.
through study completion, an average of 2 years
Elimination half-life (t1/2)
Time Frame: through study completion, an average of 2 years
To evaluate the pharmacokinetic (PK) characteristics of ICP-033 in patients with solid tumors.
through study completion, an average of 2 years
Area under plasma concentration-time curve (AUC0-t and AUC0-∞)
Time Frame: through study completion, an average of 2 years
To evaluate the pharmacokinetic (PK) characteristics of ICP-033 in patients with solid tumors.
through study completion, an average of 2 years
Apparent clearance (CL/F)
Time Frame: through study completion, an average of 2 years
To evaluate the pharmacokinetic (PK) characteristics of ICP-033 in patients with solid tumors.
through study completion, an average of 2 years
Apparent volume of distribution (Vz/F)
Time Frame: through study completion, an average of 2 years
To evaluate the pharmacokinetic (PK) characteristics of ICP-033 in patients with solid tumors.
through study completion, an average of 2 years
The objective response rate (ORR)
Time Frame: through study completion, an average of 2 years
To evaluate the preliminary anti-tumor activity of ICP-033.
through study completion, an average of 2 years
Duration of response (DoR)
Time Frame: through study completion, an average of 2 years
To evaluate the preliminary anti-tumor activity of ICP-033.
through study completion, an average of 2 years
Progression-free survival (PFS)
Time Frame: through study completion, an average of 2 years
To evaluate the preliminary anti-tumor activity of ICP-033.
through study completion, an average of 2 years
Overall survival (OS)
Time Frame: through study completion, an average of 2 years
To evaluate the preliminary anti-tumor activity of ICP-033.
through study completion, an average of 2 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Beijing InnoCare Pharma Tech Co., Ltd.

Investigators

Investigators

A researcher involved in a clinical study. Related terms include site principal investigator, site sub-investigator, study chair, study director, and study principal investigator.
  • Principal Investigator: Feng Bi, West China Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
February 25, 2022

Primary Completion (Estimated)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
December 1, 2024

Study Completion (Estimated)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
December 1, 2025

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
April 24, 2022

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
May 8, 2022

First Posted (Actual)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
May 10, 2022

Study Record Updates

Last Update Posted (Actual)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
February 7, 2024

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
February 5, 2024

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
February 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • ICP-CL-00701

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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