Clinical Study of AL2846 Capsules in the Treatment of Advanced Lung Tumor and Advanced Ovarian Cancer

Ovarian Cancer Clinical Trial

Official title:

A Multi-cohort, Randomized, Open, Multicenter Phase II Study to Evaluate the Efficacy and Safety of AL2846 Capsules in Treated Subjects With Advanced Solid Tumors

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05815862
• Other study ID #: AL2846-II-03
• Status: Recruiting
• Phase: Phase 2
• Start date: February 15, 2023
• Est. completion date: December 2024

Study information

• Verified date: September 2022
• Source: Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
• Contact: Hui Wang, Doctor
• Phone: +86 13973135460
• Email: wanghui[@]hnca.org.cn
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a multi-cohort, randomized, open, multicenter Phase II study to evaluate the efficacy and safety of AL2846 capsules in patients with advanced lung cancer and ovarian cancer. Objective response rate (ORR) and progression-free survival (PFS) are the primary endpoints.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 40
• Est. completion date: December 2024
• Est. primary completion date: June 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Subjects with advanced lung cancer or ovarian cancer confirmed by histopathology or cytology;

• Age: 18~75 years old (when signing the informed consent form); Eastern Cooperative Oncology Group (ECOG) score: 0-1;

• At least one measurable lesion according to Response Evaluation Criteria in Solid Tumours (RECIST) 1.1;

• Normal function of main organs

• The serum Human Chorionic Gonadotropin (HCG) test of female patients of childbearing age must be negative within 7 days before study enrollment and must be non-lactating; The patient should agree to use contraception during the study period and within 6 months after the end of the study period;Male subjects should agree to use contraception during the study period and for 6 months after the study period ends;

• The patient voluntarily joined the study and signed the informed consent form, with good compliance.

Exclusion Criteria:

• Combined with the following diseases or medical history:

1. Other malignant tumors have occurred or are present at the same time within<3 years before the first administration.

2. Inability to tolerate multiple factors affecting oral medication due to any reason;

3. Common Terminology Criteria for Adverse Events (CTCAE) 5.0 > grade 1 therapeutic toxicity caused by any previous treatment that has not been completely relieved, excluding hair loss;

4. Major surgical treatment or obvious traumatic injury was received within 4 weeks before the first administration;

5. The presence of unhealed wounds, fractures, gastric and duodenal active ulcers, persistent positive fecal occult-blood, ulcerative colitis, or other conditions determined by investigators that may cause gastrointestinal bleeding or perforation;

6. Arteriovenous thrombosis, such as cerebrovascular accident (including temporary ischemic attack, cerebral hemorrhage, cerebral infarction), deep vein thrombosis and pulmonary embolism, etc., occurred within 6 months before the first medication;

7. Those who have a history of psychotropic drug abuse and cannot abstain or have mental disorders;

8. Subjects with any severe and/or uncontrollable disease;

• Tumor related symptoms and treatment:

1. Had received chemotherapy, radiation, or other anticancer therapy within 4 weeks prior to first dose;

2. Within 2 weeks before the first dose, received Chinese Traditional drugs with anti-tumor indications specified in theNational Medical Products Administration (NMPA) approved drug instructions

3. Previously treated with anti-angiogenic drugs such as Cabozantinib, Anlotinib, Endostar and Bevacizumab;

4. Imaging Computed Tomography (CT)or Magnetic Resonance Imaging (MRI) shows that the tumor has invaded important blood vessels or the investigator determines that the tumor is highly likely to invade important blood vessels and cause fatal massive bleeding during the follow-up study;

5. There is a history of interstitial lung disease, severe impairment of lung function, severe pulmonary fibrosis, severe radiation pneumonia, drug-induced lung disease, and evidence of severe active lung inflammation indicated by chest CT examination during screening;

6. There are uncontrolled pleural effusion, ascites and moderate or above pericardial effusion requiring repeated drainage;

7. Patients with brain metastases accompanied by symptoms or symptoms controlled for less than 2 weeks;

• Patients who have participated in and used other antitumor investigational drugs within 4 weeks before the first dose;

• Central squamous cell carcinoma (lung cancer subjects) with great risk of hemoptysis;

• Patients with concomitant diseases that, in the opinion of the investigators, seriously endanger the safety of the patients or affect the completion of the study, or who are not suitable for inclusion for other reasons.

Related Conditions & MeSH terms

• Advanced Lung Cancer
• Carcinoma, Ovarian Epithelial
• Ovarian Cancer
• Ovarian Neoplasms

Intervention

Drug:
• AL2846 capsule
AL2846 is a multi-target tyrosine kinase inhibitor.

Locations

Country	Name	City	State
China	Hunan Cancer Hospital	Changsha	Hunan
China	The Third Xiangya Hospital of Central South University	Changsha	Hunan
China	Shanghai Pulmonary Hospital	Shanghai
China	Northern Jiangsu People's Hospital	Yangzhou	Jiangsu

Sponsors (1)

Lead Sponsor	Collaborator
Chia Tai Tianqing Pharmaceutical Group Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Objective remission rate (ORR)	ORR is defined as the percentage of subjects in complete remission (CR), partial remission (PR), and disease stability (SD).	From baseline up to 12 months.
Primary	Progression free survival (PFS)	PFS is defined as the time from randomization to the first recorded progressive disease (PD) or death from any cause.	From baseline up to 12 months.
Secondary	Disease control rate (DCR)	Percentage of subjects achieving complete response (CR) and partial response (PR).	From baseline up to 12 months.
Secondary	Duration of remission (DOR)	The time from the first evaluation as CR or PR to the first evaluation as PD or death from any cause.	From baseline up to 12 months.
Secondary	Overall survival (OS)	Time from the first administration to death from any cause.	From baseline to the death events, assessed up to 3 years.
Secondary	Adverse events (AEs) rate	Occurrence of all adverse events, regardless of whether there was a causal relation with the studied drug.	From baseline to 28 days after the last dose or initiation of a new antineoplastic therapy (whichever comes first).
Secondary	Peak concentration (Cmax)	Maximum plasma drug concentration	Pre-dose, 30 minutes, 1 hours, 2 hours, 3 hours, 4 hours, 5 hours, 6 hours, 8 hours, 12 hours and 24 hours after dose on Day 1 and Day 28 of Cycle 1. Pre-dose on Day 7, Day 14 and 21 of cycle 1. Each cycle is 28 days.
Secondary	Time to peak concentration (Tmax)	Time to reach peak plasma drug concentration after dose.	Pre-dose, 30 minutes, 1 hours, 2 hours, 3 hours, 4 hours, 5 hours, 6 hours, 8 hours, 12 hours and 24 hours after dose on Day 1 and Day 28 of Cycle 1. Pre-dose on Day 7, Day 14 and 21 of cycle 1. Each cycle is 28 days.
Secondary	Clearance half life (t1/2)	The time it takes for the drug concentration in the body to drop by half	Pre-dose, 30 minutes, 1 hours, 2 hours, 3 hours, 4 hours, 5 hours, 6 hours, 8 hours, 12 hours and 24 hours after dose on Day 1 and Day 28 of Cycle 1. Pre-dose on Day 7, Day 14 and 21 of cycle 1. Each cycle is 28 days.
Secondary	Area under blood concentration-time curve (AUC)	After administration, the area under the curve is obtained using the blood drug concentration as the ordinate and time as the abscissa.	Pre-dose, 30 minutes, 1 hours, 2 hours, 3 hours, 4 hours, 5 hours, 6 hours, 8 hours, 12 hours and 24 hours after dose on Day 1 and Day 28 of Cycle 1. Pre-dose on Day 7, Day 14 and 21 of cycle 1. Each cycle is 28 days.