A Phase Ib Study of HS-10352 Plus Fulvestrant in Patients With Advanced Breast Cancer

August 15, 2022 updated by: Jiangsu Hansoh Pharmaceutical Co., Ltd.

A Phase Ib, Open-label, Multicenter Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Efficacy of HS-10352 in Combination With Fulvestrant in Patients With Hormone Receptor (HR) Positive, Human Epidermal Growth Factor 2 (HER2)-Negative, PIK3CA Mutation, Locally Advanced or Metastatic Breast Cancer

HS-10352 is a highly potent and selective small molecule inhibitor of phosphoinositide 3-kinase (p110α). The purpose of this study is to assess the safety, tolerability, pharmacokinetics (PK), and efficacy of HS-10352 plus fulvestrant in patients with hormone receptor (HR) positive, human epidermal growth factor 2 (HER2)-negative, advanced breast cancer (ABC) harboring PIK3CA mutations.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

This is a Phase Ib open-label, 2-Part, multi-center study in China. The study will be conducted in two stages: Stage 1 is the dose-escalation part, which is designed to evaluate the safety, tolerability, PK and efficacy, as well as to determine the maximum tolerable dosage (MTD) or maximum applicable dose (MAD) of HS-10352 in combination with fulvestrant. Stage 2 is the dose-expansion part, which is aimed to further assess the efficacy, safety, tolerability and PK, and to establish the recommended phase 2 dose (RP2D) of HS-10352 in combination with fulvestrant.

All participants will be carefully monitored for adverse events (AE) during the study treatment and for 28 days after the last dose of study drug. The PK characteristics of HS-10352 and fulvestrant will be evaluated from C1 to C6. Subjects of this study will be assessed for progression once every 8 weeks until objective disease progression or withdrawal from the trial. As the disease progresses, survival follow-up is recommended bimonthly.

Study Type

Interventional

Enrollment (Anticipated)

224

Phase

  • 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 Backup

Study Locations

  • China
    • Shanghai
      • Shanghai, Shanghai, China, 200032
        • Recruiting
        • Fudan University Shanghai Cancer Center
        • Contact:
        • 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

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Men or women aged more than or equal to (≥) 18 years
  2. HR+ HER2- breast cancer confirmed by histology or cytology.
  3. Locally advanced disease not amenable to curative treatment by surgery or metastatic disease.
  4. Have adequate tumor tissue for the analysis of PIK3CA mutational status. At dose expansion stage, participants should be identified as PIK3CA-mutation positive before enrollment.
  5. Females should have postmenopausal status due to either surgical/natural menopause or ovarian suppression with a luteinizing hormone releasing hormone (LHRH) agonist before enrollment. Males should be pre-treated with a LHRH agonist.
  6. Have either measurable disease per RECIST v1.1 criteria or at least one predominantly lytic bone lesion must be present.
  7. ECOG performance status was 0-1 and did not deteriorate in the previous 2 weeks.
  8. Estimated life expectancy for at least three months

  9. Females should be using adequate contraceptive measures and should not be breastfeeding at the time of screening, during the study and until 6 months after completion of the study; and have negative results of blood pregnancy test prior to C1D1.

    Males should be using adequate contraceptive measures at the time of screening, during the study and until 6 months after completion of the study.

  10. Have signed Informed Consent Form
  11. Dose escalation stage-Cohort 1: subjects resistant to endocrine therapy Dose expansion stage-Cohort 2: subjects resistant to endocrine therapy Dose expansion stage-Cohort 3: endocrine therapy-sensitive or endocrine-naive subjects

Exclusion Criteria:

  1. Participant with symptomatic visceral disease or any disease burden that makes the participant ineligible for endocrine therapy per the investigator's best judgment

  2. Treatment with any of the following:

    1. Previous or current treatment with PI3K, AKT or mTOR inhibitors
    2. For expansion stage, prior treatment with fulvestrant
    3. Any cytotoxic chemotherapy, investigational agents within 21 days of the first dose of study drug; anticancer drugs which have been received within 14 days before the first administration.
    4. Radiotherapy with a limited field of radiation for palliation within 2 weeks of the first dose of study drug, or patients received more than 30% of the bone marrow irradiation, or large-scale radiotherapy within 4 weeks of the first dose.
    5. Major surgery (including craniotomy, thoracotomy, or laparotomy, etc.) within 4 weeks of the first dose of study drug.
  3. With inflammatory breast cancer at screening.
  4. Inadequate bone marrow reserve or organ function.
  5. Uncontrolled pleural effusion or ascites or pericardial effusion.
  6. Known and untreated, or active central nervous system metastases.
  7. History of primary or secondary diabetes.
  8. History of acute or chronic pancreatitis
  9. Refractory nausea, vomiting, or chronic gastrointestinal diseases, or inability to swallow the study drug that would preclude adequate absorption of HS-10352 or fulvestrant.
  10. History of hypersensitivity to any active or inactive ingredient of HS-10352/ fulvestrant or to drugs with a similar chemical structure or class to HS-10352.
  11. Judgment by the investigator that the patient should not participate in the study if the patient is unlikely to comply with study procedures, restrictions, and requirements.
  12. Any disease or condition that, in the opinion of the investigator, would compromise the safety of the patient or interfere with study assessments.

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: NON_RANDOMIZED
  • Interventional Model: SINGLE_GROUP
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: Cohort 1: Endocrine therapy-resistant (Stage 1)
Participants who are endocrine therapy pre-treated will be administrated at escalating doses orally of HS-10352 in combination with fulvestrant (500 mg, intramuscular).
Drug: HS-10352 combined with fulvestrant (Stage 1)

Drug: HS-10352 HS-10352 will be administered at escalating doses orally once daily on a continuous dosing schedule starting on Cycle 1 Day 1 (C1D1) in a 28 day cycle.

Drug: Fulvestrant Fulvestrant is administered at a dose of 500 mg intramuscular on Cycle 1 Day 1, Day 15, and Day 1 of every cycle thereafter (where a cycle is 28 days).
EXPERIMENTAL: Cohort 2: Endocrine therapy-resistant (Stage 2)
Participants who are endocrine therapy-resistant will be treated with HS-10352 orally at the MTD/MAD identified in Stage 1 or/and lower dose in combination with fulvestrant (500 mg, intramuscular)
Drug: HS-10352 combined with fulvestrant (Stage 2)

Drug: HS-10352 participants will be enrolled into Cohort 2 (endocrine therapy-resistant) and Cohort 3 (endocrine therapy-sensitive or naïve) respectively and HS-10352 will be administered at the recommended dose identified in Part 1.

Drug: Fulvestrant Fulvestrant is administered at a dose of 500 mg intramuscular on Cycle 1 Day 1, Day 15, and Day 1 of every cycle thereafter (where a cycle is 28 days).
EXPERIMENTAL: Cohort 3: Endocrine therapy-sensitive or endocrine-naïve (Stage 2)
Participants who are endocrine therapy-sensitive or naïve will be treated with HS-10352 orally at MTD/MAD or/and lower dose identified in Stage 1 in combination with fulvestrant (500 mg, intramuscular)
Drug: HS-10352 combined with fulvestrant (Stage 2)

Drug: HS-10352 participants will be enrolled into Cohort 2 (endocrine therapy-resistant) and Cohort 3 (endocrine therapy-sensitive or naïve) respectively and HS-10352 will be administered at the recommended dose identified in Part 1.

Drug: Fulvestrant Fulvestrant is administered at a dose of 500 mg intramuscular on Cycle 1 Day 1, Day 15, and Day 1 of every cycle thereafter (where a cycle is 28 days).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
[Stage 1] Maximum tolerated dose (MTD) of HS-10352 in combination with fulvestrant
Time Frame: Cycle 1 (28 days)
MTD is defined as the previous dose level at which 2 or more out of 2~6 subjects experienced a DLT.
Cycle 1 (28 days)
[Stage 1] Maximum applicable dose (MAD) of HS-10352 in combination with fulvestrant
Time Frame: Cycle 1 (28 days)
MAD is defined as follows: a) based on PK data, it is anticipated that at this dose level, the dose-exposure plateau has been reached, b) based on existing safety data, it is judged that dose escalation following this dose level will have a large safety risk or subject intolerance, or c) based on the PK-PD model, it suggested that the optimal target concentration of safety and efficacy has been explored.
Cycle 1 (28 days)
[Stage 2] Objective response rate (ORR) of HS-10352 in combination with fulvestrant
Time Frame: From the date of first dose until the date of disease progression or withdrawal from study, approximately 3 years
ORR is defined as the proportion of participants with best overall response (BOR) of confirmed complete response (CR) or confirmed partial response (PR) based on assessment per Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1).
From the date of first dose until the date of disease progression or withdrawal from study, approximately 3 years

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
[Stage 1 and Stage 2] Incidence and severity of treatment-emergent adverse events
Time Frame: From Cycle 1 Day 1 (C1D1) until 28 days after the final dose. A cycle is 28 days.
Assessed by number and severity of adverse events as evaluated according to NCI CTCAE v5.0.
From Cycle 1 Day 1 (C1D1) until 28 days after the final dose. A cycle is 28 days.
[Stage 1 and Stage 2] PK parameters: the maximum concentration (Cmax) of HS-10352
Time Frame: Cycle 1 Day 1 (C1D1)，at the first day of Cycle 1 (each cycle is 28 days)
Defines as the maximum plasma drug concentration of HS-10352
Cycle 1 Day 1 (C1D1)，at the first day of Cycle 1 (each cycle is 28 days)
[Stage 1] PK parameters: the maximum concentration (Cmax) of fulvestrant
Time Frame: Cycle 1 (28 days)
Defines as the maximum plasma drug concentration of fulvestrant
Cycle 1 (28 days)
[Stage 1 and Stage 2] PK parameters: time of the maximum concentration (Tmax) of HS-10352
Time Frame: Cycle 1 Day 1 (C1D1)，at the first day of Cycle 1 (each cycle is 28 days)
Defined as the time to reach maximum plasma concentration following drug administration of HS-10352
Cycle 1 Day 1 (C1D1)，at the first day of Cycle 1 (each cycle is 28 days)
[Stage 1] PK parameters: time of the maximum concentration (Tmax) of fulvestrant
Time Frame: Cycle 1 (28 days)
Defined as the time to reach maximum plasma concentration following drug administration of fulvestrant
Cycle 1 (28 days)
[Stage 1 and Stage 2] PK parameters: elimination half life (t1/2) of HS-10352
Time Frame: Cycle 1 Day 1 (C1D1)，at the first day of Cycle 1 (each cycle is 28 days)
Defines as the time measured for the concentration to decrease by one half.
Cycle 1 Day 1 (C1D1)，at the first day of Cycle 1 (each cycle is 28 days)
[Stage 1 and Stage 2] PK parameters: area under the concentration-time curve over 24 hours (AUC0-24) of HS-10352
Time Frame: Cycle 1 Day 1 (C1D1)，at the first day of Cycle 1 (each cycle is 28 days)
Defines as area under the plasma concentration versus time curve from time zero to the 24-hour sampling time.
Cycle 1 Day 1 (C1D1)，at the first day of Cycle 1 (each cycle is 28 days)
[Stage 1 and Stage 2] PK parameters: area under the concentration-time curve from time zero (pre-dose) to last time of quantifiable concentration (AUC0-t) of HS-10352
Time Frame: Cycle 1 Day 1 (C1D1)，at the first day of Cycle 1 (each cycle is 28 days)
Defines as area under the plasma concentration versus time curve from time zero to the last sampling time t at which the concentration was at or above the lower limit of quantification (LLOQ).
Cycle 1 Day 1 (C1D1)，at the first day of Cycle 1 (each cycle is 28 days)
[Stage 1] PK parameters: area under the concentration-time curve from time zero (pre-dose) to last time of quantifiable concentration (AUC0-t) of fulvestrant
Time Frame: From Cycle 1 to Cycle 2， each cycle is 28 days
Defines as area under the plasma concentration versus time curve from time zero to the last sampling time t at which the concentration was at or above the lower limit of quantification (LLOQ).
From Cycle 1 to Cycle 2， each cycle is 28 days
[Stage 1 and Stage 2] PK parameters: the maximum concentration at steady-state (Css,max) of HS-10352
Time Frame: Cycle 2 Day 1 (C2D1)，at the first day of Cycle 2 (each cycle is 28 days) each cycle is 28 days
Defines as the maximum plasma drug concentration of HS-10352 at steady-state
Cycle 2 Day 1 (C2D1)，at the first day of Cycle 2 (each cycle is 28 days) each cycle is 28 days
[Stage 1] PK parameters: the maximum concentration at steady-state (Css,max) of fulvestrant
Time Frame: Cycle 2 (28 days)
Defines as the maximum plasma drug concentration of fulvestrant at steady-state
Cycle 2 (28 days)
[Stage 1 and Stage 2] PK parameters: time of the maximum concentration at steady state (Tss,max) of HS-10352
Time Frame: Cycle 2 Day 1 (C2D1)，at the first day of Cycle 1 (each cycle is 28 days)
Defined as the time to reach maximum plasma concentration following drug administration of HS-10352 at steady-state
Cycle 2 Day 1 (C2D1)，at the first day of Cycle 1 (each cycle is 28 days)
[Stage 1] PK parameters: time of the maximum concentration at steady state (Tss,max) of fulvestrant
Time Frame: Cycle 2 (28 days)
Defined as the time to reach maximum plasma concentration following drug administration of fulvestrant at steady-state
Cycle 2 (28 days)
[Stage 1 and Stage 2] PK parameters: the minimum concentration at steady-state (Css,min) of HS-10352
Time Frame: Cycle 2 Day 1 (C2D1)，at the first day of Cycle 1 (each cycle is 28 days)
Defines as the minimum plasma drug concentration of HS-10352 at steady-state
Cycle 2 Day 1 (C2D1)，at the first day of Cycle 1 (each cycle is 28 days)
[Stage 1 and Stage 2] PK parameters: the minimum concentration at steady-state (Css,min) of fulvestrant
Time Frame: Cycle 2 (28 days)
Defines as the minimum plasma drug concentration of fulvestrant at steady-state
Cycle 2 (28 days)
[Stage 1] Efficacy of HS-10352 in combination with fulvestrant: ORR
Time Frame: From the date of first dose until the date of disease progression or withdrawal from study, approximately 3 years
ORR is defined as the proportion of participants with BOR of confirmed CR or confirmed PR based on assessment per RECIST v1.1.
From the date of first dose until the date of disease progression or withdrawal from study, approximately 3 years
[Stage 1 and Stage 2] Efficacy of HS-10352 in combination with fulvestrant: disease control rate (DCR)
Time Frame: From the date of first dose until the date of disease progression or withdrawal from study, approximately 3 years
The disease control was defined as the percentage of patients who have a best overall response (confirmed CR, PR, or stable disease for at least 6 weeks).
From the date of first dose until the date of disease progression or withdrawal from study, approximately 3 years
[Stage 1 and Stage 2] Efficacy of HS-10352 in combination with fulvestrant: duration of response (DoR)
Time Frame: From the date of CR, PR until the date of disease progression or withdrawal from study, approximately 3 years
DOR only applies to participants whose best overall response is CR or PR based on assessment per RECIST v1.1. The start date is the date of first documented response of CR or PR (i.e. the start date of observed response, not the date when response was confirmed), and the end date is defined as the date of the first documented progression or death due to underlying cancer.
From the date of CR, PR until the date of disease progression or withdrawal from study, approximately 3 years
[Stage 1 and Stage 2] Efficacy of HS-10352 in combination with fulvestrant: progression free survival (PFS)
Time Frame: From the date of randomization or first dose (if randomization is not needed) until the date of disease progression or withdrawal from study, approximately 3 years
PFS is defined as the time from the date of randomization or first dose (if randomization is not needed) to the date of the first documented progression or death due to any cause. PFS will be assessed per RECIST v1.1.
From the date of randomization or first dose (if randomization is not needed) until the date of disease progression or withdrawal from study, approximately 3 years
[Stage 2] Efficacy of HS-10352 in combination with fulvestrant: overall survival (OS)
Time Frame: From the date of randomization or first dose (if randomization is not needed) until the documentation of death from any cause, approximately 6 years
OS is defined as the time from the date of randomization or first dose (if randomization is not needed) to the date of death due to any cause. For each participant who is not known to have died as of the cutoff date for overall survival analysis, OS time was censored on the last date the participant is known to be alive.
From the date of randomization or first dose (if randomization is not needed) until the documentation of death from any cause, approximately 6 years

Collaborators and Investigators

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

Sponsor

Jiangsu Hansoh Pharmaceutical Co., Ltd.

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)

January 12, 2022

Primary Completion (ANTICIPATED)

July 31, 2023

Study Completion (ANTICIPATED)

December 31, 2025

Study Registration Dates

First Submitted

May 17, 2022

First Submitted That Met QC Criteria

August 15, 2022

First Posted (ACTUAL)

August 17, 2022

Study Record Updates

Last Update Posted (ACTUAL)

August 17, 2022

Last Update Submitted That Met QC Criteria

August 15, 2022

Last Verified

May 1, 2022

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • HS-10352-102

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.

Clinical Trials on Breast Cancer

Clinical Trials on HS-10352 combined with fulvestrant (Stage 1)

Search Similar Trials

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Croatia

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations

Subscribe