A Phase I/IIa Study of AL8326 Combined With Toripalimab in the Treatment of Advanced Solid Tumors.

Recruiting now · Phase 1/Phase 2

Conditions studied: Solid Tumor

In brief

This trial is an open, non-randomized, phase I/IIa clinical trial, which will evaluate the preliminary effectiveness and safety of AL8326 tablets in patients with advanced solid tumors

Key facts

Study ID

NCT07392736

Run by

Advenchen Laboratories, LLC

People needed

228

Starts

2021-10-26

Expected to finish

2029-11-07

Last updated by the study team

2026-02-06

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects must be able to understand and voluntarily sign a written informed consent form prior to the initiation of any study-related procedures.
• Age ≥ 18 years.
• Subjects with histologically confirmed advanced recurrent or metastatic solid tumors who meet one of the following conditions:
• Failure of standard therapy (disease progression after treatment or intolerance to treatment toxicity);
• no effective treatment available.
• Toripalimab monotherapy as a second-line or later standard treatment.
• Must have at least one measurable lesion as defined by RECIST 1.1.
• Prior cytotoxic chemotherapy must have been completed at least 4 weeks before enrollment, and any toxicities must have recovered to ≤ Grade 1 (except alopecia).
• Life expectancy of ≥ 12 weeks at the time of enrollment.
• ECOG performance status of 0 or 1.
• Adequate organ function:
• Bone marrow function: Absolute neutrophil count (ANC) ≥ 1.5 × 10⁹/L (1500/mm³); Platelets ≥ 100 × 10⁹/L; Hemoglobin ≥ 9.0 g/dL.
• Renal function: Serum creatinine ≤ 1.5 × upper limit of normal (ULN) or calculated creatinine clearance (Cockcroft-Gault formula) ≥ 60 mL/min.
• Hepatic function: Total bilirubin ≤ 1.5 × ULN (≤ 3.0 × ULN for subjects with Gilbert's syndrome); AST and ALT ≤ 2.5 × ULN in subjects without liver metastases, or ≤ 5 × ULN in subjects with liver metastases.
• Coagulation function: International normalized ratio (INR) ≤ 1.5; Activated partial thromboplastin time (APTT) ≤ 1.5 × ULN.
• Left ventricular ejection fraction (LVEF) > 50% during screening.
• Systolic blood pressure < 140 mmHg and diastolic blood pressure < 90 mmHg (without medication or controlled with a single agent).
• Females: Women of childbearing potential must have a negative serum pregnancy test within 7 days prior to enrollment and must agree to use medically acceptable methods of contraception during the treatment period and for 3 months after the last dose; The patient must be non-lactating; Postmenopausal women (≥ 12 months of amenorrhea without other causes) or surgically sterilized (oophorectomy and/or hysterectomy) are not considered of childbearing potential. Their partners must use medically acceptable contraception during the treatment period and for 3 months after the last dose. Males: Surgically sterile or must agree to use medically acceptable contraception during the treatment period and for 3 months after the last dose; Their partners must use medically acceptable contraception during the same period.
• Ability and willingness to comply with the study protocol for the duration of the study and with follow-up procedures.

You may not qualify if…

• Received systemic cytotoxic therapy or investigational therapy within 28 days prior to initiation of study treatment, or non-cytotoxic, non-investigational therapy (e.g., radiotherapy, hormone therapy, targeted therapy, immunotherapy) within 14 days prior to initiation of study treatment.
• Major surgery (defined as requiring general anesthesia within 28 days before initiation of study treatment, or minor surgery requiring general anesthesia within 7 days before initiation of study treatment).
• Pregnant or lactating women.
• History of prior or concurrent second primary malignancy that, in the opinion of the investigator or sponsor, may interfere with the assessment of safety or efficacy of the study treatment.
• Subjects with active or untreated central nervous system (CNS) metastases; Subjects with stable brain metastases may be enrolled if they meet the following criteria: a) No radiological evidence of progression for ≥ 4 weeks after completion of treatment; b) Completion of treatment ≥ 28 days before the first dose of study drug; c) No requirement for systemic corticosteroids (>10 mg/day prednisone or equivalent) within ≤ 14 days prior to the first dose of study drug.
• Active, known, or suspected autoimmune disease or interstitial lung disease.
• Requirement for systemic therapy with corticosteroids or other immunosuppressive drugs within 14 days prior to initiation of study treatment.
• Peptic ulcer disease, inflammatory bowel disease, ulcerative colitis, or other gastrointestinal conditions with risk of perforation; History of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 28 days prior to initiation of study treatment.
• Untreated deep vein thrombosis (DVT) within the past 6 months. Subjects with DVT treated with therapeutic anticoagulants (excluding therapeutic warfarin) for at least 14 days prior to initiation of study treatment are allowed.
• Uncontrolled infection.
• New York Heart Association (NYHA) Grade III or greater congestive heart failure.
• History of any of the following cardiac conditions within 6 months prior to initiation of study treatment:
• Cardiac angioplasty or stenting;
• Myocardial infarction;
• Unstable angina;
• Cerebrovascular accident.
• Presence of any unhealed wound, fracture, or ulcer, or symptomatic peripheral vascular disease.
• Evidence of hemorrhagic diathesis, coagulation disorder, or clinically significant bleeding (e.g., severe hematuria, gastrointestinal bleeding, hemoptysis) within 6 months prior to initiation of study treatment.
• QTcF ≥470 msec on screening ECG per Fridericia's formula.
• Urinalysis showing urine protein ≥ ++ and 24-hour urine protein quantification > 1.0 g within 28 days prior to initiation of study treatment.
• Positive hepatitis B surface antigen (HBsAg) with HBV-DNA above the lower limit of detection of the local laboratory; Positive hepatitis C antibody (anti-HCV) with HCV-RNA above the lower limit of detection of the local laboratory; Positive syphilis antibody; Positive human immunodeficiency virus (HIV) antibody test.
• History of organ transplantation.
• Clinical conditions affecting the intake or absorption of AL8326 (e.g., inability to swallow, chronic diarrhea, intestinal obstruction, malabsorption disorders, gastrectomy or small bowel resection).
• Use of prohibited concomitant medications within 14 days prior to initiation of study treatment.
• Receipt of red blood cell or platelet transfusion within 14 days prior to initiation of study treatment.

Where it is running

• National GCP Center for Anticancer Drugs,The Independent Ethics Committee — Beijing, Beijing Municipality, China (enrolling)
• The Cancer Hospital of the Chinese Academy of Medical Sciences — Beijing, Beijing Municipality, China (enrolling)
• Hunan Cancer Hospital — Hunan, Changsha, China (enrolling)
• Fujian Cancer Hospital — Fuzhou, Fujian, China (enrolling)
• Cancer Hospital of Shantou University Medical College — Shantou, Guangdong, China (enrolling)
• Yuebei People's Hospital — Shaoguan, Guangdong, China (enrolling)
• The First Affiliated Hospital of Guilin Medical Universty — Guilin, Guangxi, China (enrolling)
• Liuzhou Workers' Hospital — Liuzhou, Guangxi, China (enrolling)
• The People's Hospital of Guangxi Zhuang Autonomous Region — Nanning, Guangxi, China (enrolling)
• Guangxi Medical University Cancer Hospital — Nanning, Guangxi, China (enrolling)
• Henan Cancer Hospital — Zhengzhou, Henan, China (enrolling)
• The First Affiliated Hospital of Zhengzhou University — Zhengzhou, Henan, China (enrolling)
• The First Affiliated Hospital of Xi'an Jiaotong University — Xi’an, Shanxi, China (enrolling)
• Zhejiang Cancer Hospital — Hangzhou, Zhejiang, China (enrolling)
• SIR RUN RUN SHAW Hospital Zhejiang University School Of Medicine — Hangzhou, Zhejiang, China (enrolling)

Full record on ClinicalTrials.gov

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