RECRUITING

A Study of AND019 in Women With ER Positive HER2 Negative Advanced or Metastatic Breast Cancer

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This is a first in human dose escalation and expansion study to evaluate the safety, tolerability, pharmacokinetic (PK), pharmacodynamic (PD) activity, and preliminary anti-tumor activity of AND019 in postmenopausal women with advanced or metastatic estrogen receptor (ER)-positive (human epidermal growth factor receptor 2 \[HER2\]-negative) breast cancer.

Official Title

A Phase I Dose Escalation and Dose Expansion Study of AND019 in Patients With Estrogen Receptor Positive Human Epidermal Growth Factor Receptor 2 Negative Advanced or Metastatic Breast Cancer

Quick Facts

Study Start:2022-10-05

Study Completion:2026-05

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT05187832

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.

Ages Eligible for Study:18 Years

Sexes Eligible for Study:FEMALE

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
1. Postmenopausal women defined as NCCN guideline at the time of informed consent. 2. Histological or cytological confirmation of advanced or metastatic ER+/HER2- breast cancer women who failed standard therapy or for which no standard therapy exists. 3. Prior therapy: 1. No more than 1 line of chemotherapy for advanced breast cancer 2. Recurrence or progression on at least one line of endocrine therapy in the advanced or metastatic disease setting and derived a clinical benefit from the endocrine therapy: Recurred or progressed while being treated with adjuvant endocrine therapy for a duration of at least 24 months, or progressed under endocrine therapy for more than 6 months in the advanced or metastatic setting 4. ECOG score 0-1. 5. Minimum life expectancy of a least 3 months as determined by the Investigator. 6. Evaluable disease per RECIST 1.1; for patients consent to tissue biopsy, disease suitable for tumor biopsy. 7. Sufficient bone marrow reserve and organ function.	1. Previous treatment with any SERDs. 2. Patient any central nervous system metastasis. 3. Prior antitumor therapies: 1. Received chemotherapies within 3 weeks before the first dose. 2. Received systemic radiotherapy within 3 weeks before the first dose, or local radiotherapy within 7 days before the first dose 3. Received other anti-tumor therapy such as endocrine therapy, immunotherapy, and target therapy within 3 weeks or 5 half-lives of the drug before the first dose of the study drug 4. For bone metastasis, bisphosphonates and local remission therapy are allowed (7 days washout for local radiation therapy). 4. Patient who has participated in any other clinical trials for drugs or treatments within 5 half-lives for a prior investigational drug or 2 weeks from use of an investigational device prior to the first dose of study drug. 5. Patient who had major surgery or significant trauma within 4 weeks prior to the first dose of study drug (excluding needle biopsy), or has scheduled surgery during the study period. 6. Patient with serous unhealable wounds/ulcers/fractures within 4 weeks prior to the first dose of study drug. 7. Patient with adverse reactions to previous anti-tumor treatments who have not yet recovered to grade ≤1 according to CTCAE v5.0. (except for toxicities without safety risks as judged by Investigator, such as alopecia, grade 2 peripheral neuropathy etc.) 8. Patient who has used strong inhibitors or strong inducers of CYP3A, or grapefruit or grapefruit juice within 4 weeks prior to the first dose of study drug. 9. Patient unable to be administered oral medications or any condition that seriously affect digestion in the gastrointestinal tract at the judgement of the Investigator. 10. Patient with active infection within 1 week prior to the first dose of study drug, and currently need systemic anti-infective treatment. 11. Patient has a known history of the following: HIV infection without effective antiretroviral therapy (ART) or acceptable immune function, or syphilis infection, or HBsAg positive HBV or needs prophylaxis therapy or suppressive antiviral therapy before dosing, or has an HCV infection that hasn't completed curative antiviral treatment or with unacceptable viral load. 12. Patient has active cardiac disease or a history cardiac dysfunction. 13. Patient with third spacing that cannot be controlled clinically and is not suitable for the study by the Investigator's judgment. 14. Patient with known history of drug abuse. 15. Patient with mental disorder that, in the opinion of the Investigator, could lead to poor compliance with required study procedures. 16. Patient that cannot tolerate venous blood sampling. 17. Known to have other malignancy within the past 5 years, and is progressing or requires active treatment (except skin basal cell carcinoma, squamous cell carcinoma, or cervical carcinoma in situ who have received potentially radical treatment)

Inclusion Criteria

Exclusion Criteria

1. Postmenopausal women defined as NCCN guideline at the time of informed consent.
2. Histological or cytological confirmation of advanced or metastatic ER+/HER2- breast cancer women who failed standard therapy or for which no standard therapy exists.
3. Prior therapy:
1. No more than 1 line of chemotherapy for advanced breast cancer
2. Recurrence or progression on at least one line of endocrine therapy in the advanced or metastatic disease setting and derived a clinical benefit from the endocrine therapy: Recurred or progressed while being treated with adjuvant endocrine therapy for a duration of at least 24 months, or progressed under endocrine therapy for more than 6 months in the advanced or metastatic setting
4. ECOG score 0-1.
5. Minimum life expectancy of a least 3 months as determined by the Investigator.
6. Evaluable disease per RECIST 1.1; for patients consent to tissue biopsy, disease suitable for tumor biopsy.
7. Sufficient bone marrow reserve and organ function.

1. Previous treatment with any SERDs.
2. Patient any central nervous system metastasis.
3. Prior antitumor therapies:
1. Received chemotherapies within 3 weeks before the first dose.
2. Received systemic radiotherapy within 3 weeks before the first dose, or local radiotherapy within 7 days before the first dose
3. Received other anti-tumor therapy such as endocrine therapy, immunotherapy, and target therapy within 3 weeks or 5 half-lives of the drug before the first dose of the study drug
4. For bone metastasis, bisphosphonates and local remission therapy are allowed (7 days washout for local radiation therapy).
4. Patient who has participated in any other clinical trials for drugs or treatments within 5 half-lives for a prior investigational drug or 2 weeks from use of an investigational device prior to the first dose of study drug.
5. Patient who had major surgery or significant trauma within 4 weeks prior to the first dose of study drug (excluding needle biopsy), or has scheduled surgery during the study period.
6. Patient with serous unhealable wounds/ulcers/fractures within 4 weeks prior to the first dose of study drug.
7. Patient with adverse reactions to previous anti-tumor treatments who have not yet recovered to grade ≤1 according to CTCAE v5.0. (except for toxicities without safety risks as judged by Investigator, such as alopecia, grade 2 peripheral neuropathy etc.)
8. Patient who has used strong inhibitors or strong inducers of CYP3A, or grapefruit or grapefruit juice within 4 weeks prior to the first dose of study drug.
9. Patient unable to be administered oral medications or any condition that seriously affect digestion in the gastrointestinal tract at the judgement of the Investigator.
10. Patient with active infection within 1 week prior to the first dose of study drug, and currently need systemic anti-infective treatment.
11. Patient has a known history of the following: HIV infection without effective antiretroviral therapy (ART) or acceptable immune function, or syphilis infection, or HBsAg positive HBV or needs prophylaxis therapy or suppressive antiviral therapy before dosing, or has an HCV infection that hasn't completed curative antiviral treatment or with unacceptable viral load.
12. Patient has active cardiac disease or a history cardiac dysfunction.
13. Patient with third spacing that cannot be controlled clinically and is not suitable for the study by the Investigator's judgment.
14. Patient with known history of drug abuse.
15. Patient with mental disorder that, in the opinion of the Investigator, could lead to poor compliance with required study procedures.
16. Patient that cannot tolerate venous blood sampling.
17. Known to have other malignancy within the past 5 years, and is progressing or requires active treatment (except skin basal cell carcinoma, squamous cell carcinoma, or cervical carcinoma in situ who have received potentially radical treatment)

Contacts and Locations

Study Contact

Yusha Zhu, MD PhD

CONTACT

6467252552

yushazhu@kindpharmaceutical.com

Principal Investigator

Yusha Zhu, MD PhD

STUDY_DIRECTOR

Kind Pharmaceuticals LLC

Study Locations (Sites)

Sarah Cannon Research Institute

Nashville, Tennessee, 37203

United States

Collaborators and Investigators

Sponsor: Kind Pharmaceuticals LLC

Yusha Zhu, MD PhD, STUDY_DIRECTOR, Kind Pharmaceuticals LLC

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 Registration Dates

Study Start Date2022-10-05

Study Completion Date2026-05

Study Record Updates

Study Start Date2022-10-05

Study Completion Date2026-05

Terms related to this study

Additional Relevant MeSH Terms

Advanced or Metastatic Breast Cancer