Safety of GQ1001 in Adult Patients With HER2-Positive Advanced Solid Tumors

HER2-positive Breast Cancer Clinical Trial

Official title:

A Phase 1, First-In-Human, Multicenter, Open-Label, Study of GQ1001, a HER2 Targeted Antibody-Drug Conjugate, Administered Intravenously, in Adult Patients With HER2-Positive Advanced Solid Tumors

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04450732
• Other study ID #: GQ1001X2101
• Status: Recruiting
• Phase: Phase 1
• Start date: July 7, 2020
• Est. completion date: May 1, 2024

Study information

• Verified date: November 2023
• Source: GeneQuantum Healthcare (Suzhou) Co., Ltd.
• Contact: Yan Shi
• Phone: 0512-66526166
• Email: shiy[@]genequantum.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Phase I Dose Finding Study for GQ1001 in Patients with HER2-Positive Advanced Solid Tumors

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 96
• Est. completion date: May 1, 2024
• Est. primary completion date: March 1, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Signed informed consent form and able to comply with the protocol;

2. Male and female subjects =18 years of age;

3. ECOG PS of 0 or 1, the estimated life expectancy = 3 months;

4. LVEF = 50% as determined by echocardiography (ECHO);

5. Patients must have pathologically documented advanced/unresectable or metastatic solid tumor with HER2-positive (as defined below) that is relapsed or refractory to standard therapy or for which there is no standard therapy and progressed. Patients must have a least one measurable disease lesion. Tumor specimens to identify HER2 status should be obtained within the past 6 months.

Definition of HER2-positive

• Advanced/unresectable or metastatic breast cancer: immunohistochemistry (IHC) 3+, or IHC 2+ and in situ hybridization positive (ISH+)*;

• Advanced/unresectable or metastatic gastric or gastroesophageal junction adenocarcinoma: IHC 3+, or IHC 2+ and ISH+*;

• Other HER2-positive advanced/unresectable or metastatic solid malignant tumor:

determined by IHC, ISH, Next Generation Sequencing, or other analysis techniques as appropriate;

• ISH: fluorescence in situ hybridization (FISH) or dual in situ hybridization (DISH); ISH positivity is defined as a ratio of = 2.0 for the number of HER2 gene copies to the number of signals for CEP17. ISH assay is not required when IHC result is 3+. ISH assay should be performed to confirm HER2 positivity when IHC result is 2+.

6. Adequate organ function confirmed at screening and within 7 days before the first treatment, as evidenced by:

Platelet count: = 100,000/mm3 ; Hemoglobin : = 9 g/dL; Absolute neutrophil count (ANC): = 1500/mm3 ; Serum creatinine: = 1.5 × ULN (upper limit of normal), or creatinine clearance = 60 mL/min (using Cockcroft Gault formula) ; Aspartate aminotransferase (AST)/alanine aminotransferase (ALT) : = 2.5 × ULN (= 5 × ULN if liver metastases are present); Total bilirubin : = 1.5 × ULN (except for patients with Gilbert's Syndrome); Prothrombin time and activated partial thromboplastin time: = 1.5 × ULN.

7. Adequate washout period before the first treatment as defined by:

Major surgery: = 4 weeks. Radiation therapy: = 4 weeks (= 2 weeks for palliative stereotactic radiation therapy without abdominal). Autologous transplantation: = 3 months.

Hormonal therapy: = 2 weeks or per Investigator's discretion for breast cancer patients.

Chemotherapy or targeted therapy (including antibody drug therapy): = 3 weeks (= 2 weeks for 5 flourouracil-based agents, folinate agents, and/or weekly paclitaxel; = 2 weeks (or 5 half-lives, whichever is shorter) for tyrosine kinase inhibitors; = 4 weeks for HER2-directed biologic therapies; = 6 weeks for nitrosoureas or mitomycin C). Immunotherapy: = 4 weeks. Strong cytochrome P450 enzyme 3A4 (CYP3A4) inhibitor: = 3 elimination half-lives . Any investigational agents or treatments: = 4 weeks.

8. Patients without a history of acquired immunodeficiency syndrome (AIDS)-defining opportunistic infections or with a history of AIDS-defining opportunistic infections and have not had an opportunistic infection within the past 12 months may be enrolled per the discretion of the Investigator.

Exclusion Criteria:

1. Clinically active brain metastases, defined as untreated and symptomatic, or requiring therapy with steroids or anticonvulsants to control associated symptoms. Subjects with treated brain metastases that are no longer symptomatic and who require no treatment with steroids may be included in the study if they have recovered from the acute toxic effect of chemotherapy or radiotherapy;

2. Subjects with multiple primary malignancies within 2 years, except adequately resected non-melanoma skin cancer, curatively treated in situ disease, other solid tumors curatively treated, or contralateral breast cancer);

3. Cardiovascular dysfunction or clinically significant cardiac disease, including but not limited to:

• Medical history of symptomatic chronic heart failure (New York Heart Association (NYHA) classes II-IV) or serious cardiac arrhythmia requiring treatment;

• Medical history of myocardial infarction or unstable angina within 6 months of the first treatment;

• Corrected QT interval by Fridericia (QTcF) prolongation of > 450 milliseconds (ms) in males and > 470 ms in females;

4. Medical history of clinically significant lung disease (e.g., interstitial pneumonia, pneumonitis, pulmonary fibrosis, and severe radiation pneumonitis), or patients who are suspected to have these diseases by imaging at screening or requirement for supplemental oxygen;

5. Known hypersensitivity to either the drug substances or inactive ingredients in the drug product;

6. Existing Grade = 2 peripheral neuropathy;

7. Unresolved toxicities from previous anticancer therapy, defined as toxicities (other than alopecia) not yet resolved to NCI CTCAE version 5.0, Grade = 1 or baseline. Subjects with chronic Grade 2 toxicities may be eligible per the discretion of the Investigator;

8. Cumulative anthracycline dose > 360 mg/m2 doxorubicin or equivalent;

9. Uncontrolled infection requiring i.v. of antibiotics, antivirals or antifungals;

10. Active infection with hepatitis C (e.g., detectable antibodies to hepatitis C virus [HCV]) or hepatitis B (e.g., hepatitis B surface antigen [HBsAg] positive) except subjects with occult or prior hepatitis B infection (defined as positive total hepatitis B core antibody and negative HBsAg) may be included if hepatitis B virus (HBV) deoxyribonucleic acid (DNA) is undetectable at the time of screening, and these subjects must be willing to undergo monthly DNA testing and appropriate antiviral therapy as indicated;

11. Patients with a history or current evidence of any concomitant condition, therapy, or laboratory abnormality that, in the opinion of the Investigator, might confound the results of the trial, interfere with the patient's participation and compliance;

12. Women who are lactating or pregnant, as confirmed by pregnancy test within 7 days before first treatment;

13. Male and female subjects who are unwilling to use adequate contraceptive methods (e.g., concomitant use of a spermicidal agent, barrier contraceptive, or/and intrauterine contraceptive) during the study and for at least 7 months after the last dose of GQ1001.

Related Conditions & MeSH terms

• Biliary Tract Neoplasms
• HER2-positive Breast Cancer

Intervention

Drug:
• GQ1001
anti-HER2 antibody drug conjugate

Locations

Country	Name	City	State
Australia	Cabrini Institute in Melbourne, Australia	Melbourne	Victoria
Australia	Scientia Clinical Research Limited	Randwick	New South Wales
China	Beijing Tongren Hospital Affiliated to Capital University of Medical Sciences	Beijing	Beijing
China	Chinese PLA general hospital	Beijing	Beijing
China	The first affiliated hospital of Bengbu medical college	Bengbu	Anhui
China	Hunan Cancer Hospital	Changsha	Hunan
China	West China School of Medicine and West China Hospital, Sichuan University	Chengdu	Sichuan
China	Southern Medical University Hospital in the south	Guangzhou	Guangdong
China	Sun Yat-sen Memorial Hospital	Guangzhou	Guangdong
China	First Affiliated Hospital of Zhejiang University School of Medicine	Hangzhou	Zhejiang
China	Zhejiang Cancer Hospital	Hangzhou	Zhejiang
China	Shandong Tumor Hospital	Jinan	Shandong
China	Changhai Hospital of Shanghai	Shanghai	Shanghai
China	Ruijin Hospital, Affiliated to Shanghai Jiaotong University	Shanghai	Shanghai
China	Shanghai East Hospital	Shanghai	Shanghai
China	Shanghai Ninth People's Hospital affiliated with the Shanghai Jiao Tong University School of Medicine	Shanghai	Shanghai
China	Shanghai Pulmonary Hospital	Shanghai	Shanghai
China	Zhongshan Hospital	Shanghai	Shanghai
China	Liaoning Cancer Hospital & Institute	Shenyang	Liaoning
China	Hubei Cancer Hospital	Wuhan	Hubei
China	Hubei Huazhong University of Science and provincial Cancer Hospital Affiliated Union Hospital of Tongji Medical College	Wuhan	Hubei
China	Henan Cancer Hospital	Zhengzhou	Henan
China	The First Affiliated Hospital of Zhengzhou University	Zhengzhou	Henan
United States	M.D. Anderson Cancer Center	Houston	Texas

Sponsors (1)

Lead Sponsor	Collaborator
GeneQuantum Healthcare (Suzhou) Co., Ltd.

Countries where clinical trial is conducted

United States,  Australia,  China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Dose Limiting Toxicities (DLTs).	Adverse events will be assessed using NCI CTCAE version 5.0 and will be evaluated by the investigator and the sponsor for the eligibility of DLT.	End of Cycle 1 (21-day cycle)
Primary	Maximum Tolerated Dose (MTD) or Dose Recommended for Dose Expansion (DRDE)	The SRC will also determine the MTD/DRDE based on the totality of data for all tested dose levels.	After each cohort completes the DLT observation period (Day 1 to Day 21 after the first dose of study treatment) or has a DLT or becomes not DLT-evaluable
Secondary	Incidence and Severity of Adverse Events (AEs)	Safety and Tolerability of GQ1001	from baseline to 30 days after last dose
Secondary	Number of Participants with Abnormal Laboratory Values	Safety and Tolerability of GQ1001	rom baseline through Cycle 8 (each cycle is 21 days) and up to 30 days from treatment discontinuationafter last dose
Secondary	Area Under the Plasma Concentration Versus Time Curve (AUC) of GQ1001		through study completion, an average of 1 year
Secondary	Peak Plasma Concentration of GQ1001 (Cmax)		through study completion, an average of 1 year
Secondary	Time at which the Cmax is Observed (Tmax)		through study completion, an average of 1 year
Secondary	Half Life of GQ1001 (T1/2)		through study completion, an average of 1 year
Secondary	Mean Residence Time of GQ1001 (MRT)		through study completion, an average of 1 year
Secondary	Volume of Distribution of GQ1001 (Vd)		through study completion, an average of 1 year
Secondary	Preliminary Efficacy of GQ1001 Evaluated using Response Evaluation Criteria in Solid Tumors (RECIST 1.1) and CT of MRI scans		through study completion, an average of 1 year
Secondary	Immunogenicity	Anti-GQ1001 antibody/anti-therapeutic antibody	through study completion, an average of 1 year
Secondary	Preliminary Efficacy	objective response rate (ORR)	through study completion, an average of 1 year
Secondary	Preliminary Efficacy	disease control rate (DCR)	through study completion, an average of 1 year
Secondary	Preliminary Efficacy	duration of response (DoR)	through study completion, an average of 1 year
Secondary	Preliminary Efficacy	progression-free survival (PFS)	through study completion, an average of 1 year