- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04970914
Anlotinib Plus Penpulimab (AK105) for Chemo-refractory Metastatic Colorectal Cancer:ALTER-C003 (ALTER-C003)
March 6, 2022 updated by: YueJuan Cheng, Peking Union Medical College Hospital
Anlotinib Hydrochloride In Combination With Penpulimab (AK105) in Patients With Chemo-refractory Metastatic Colorectal Cancer, Open, Single Arm,Exploratory Clinical Trial(ALTER-C003)
A single-arm, open-label clinical trial, focus on the safety and efficacy of anlotinib hydrochloride in combination with Penpulimab (AK105) in patients with Chemo-refractory Metastatic Colorectal Cancer (mCRC)
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
32
Phase
- Phase 2
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
- Name: Jianfeng Zhou
- Phone Number: 011-86-10-69156114
- Email: ZhouJF@pumch.cn
Study Locations
-
-
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Beijing, China
- Recruiting
- Peking Union Medical College Hospital
-
Contact:
- jianfeng Zhou
- Email: ZhouJF@pumch.cn
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Shenyang, China
- Not yet recruiting
- The First Hospital of China Medical University
-
Contact:
- Xiujuan Qu
-
Shenyang, China
- Not yet recruiting
- The People's Hospital of Liaoning Province
-
Contact:
- Du Zhenguang
-
-
Beijing
-
Beijing, Beijing, China
- Recruiting
- Beijing Tiantan Hospital, Capital Medical University
-
Contact:
- Xiaoyuan Li
-
Principal Investigator:
- Xiaoyuan Li
-
Beijing, Beijing, China
- Not yet recruiting
- China-Japan Friendship Hospital
-
Principal Investigator:
- Yuan Li
-
Contact:
- Yuan Li
-
-
Hebei
-
Langfang, Hebei, China
- Not yet recruiting
- Hebei Petro China Central Hospital
-
Contact:
- Qian Guo
-
Principal Investigator:
- Qian Guo
-
Shijiazhuang, Hebei, China
- Not yet recruiting
- The Fourth Hospital of Hebei Medical University (Hebei Cancer Hospital)
-
Principal Investigator:
- Ruixing Zhang
-
Contact:
- Ruixing Zhang
- Phone Number: 0086-311-86095757
-
-
Tianjin
-
Tianjin, Tianjin, China
- Recruiting
- General Hospital of Tianjin Medical University
-
-
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:
- Patients participate in the study voluntarily and sign informed consent with good compliance.
- Be 18 years of age or older on day of signing informed consent.
- Histological or cytological confirmation of Metastatic Colorectal Cancer(T1-4N0-2M1).
- At least one measurable lesion, with diameter ≥ 10mm measured by spiral MRI/CT scan per RECIST1.1.
- Participants must have received and progressed through or become intolerant to fluoropyrimidine, irinotecan, oxaliplatin, Exceptions may apply.
- Eastern Cooperative Oncology Group Performance Status 0 or 1.
- Life expectancy of at least 3 months.
- Main organs function is normal. (normal main organs function as defined below: Hemoglobin (Hb) ≥ 90 g/L, Neutrophils (ANC) ≥ 1.5×109/L, leucocyte (WBC) ≥ 3.0×109/L,Platelet count (PLT) ≥ 75×109/L,Total bilirubin (TBIL) ≤ 1.5 × normal upper limit (ULN), Aspartate aminotransferase (AST) and Alanine aminotransferase (ALT) ≤ 2.5 ×ULN, If liver metastasis is present,ALT and AST<5ULN ;Serum creatinine (Cr) ≤ 1.5× ULN or Creatinine Clearance rate(CCr) ≥60ml/min,Doppler ultrasound evaluation: left ventricular ejection fraction (LVEF) > 50%)
- The woman patients of childbearing age who must agree to take contraceptive methods (e.g. intrauterine device, contraceptive pill or condom) during the research and within another 3 months after it; who are not in the lactation period and examined as negative in blood serum test or urine pregnancy test within 7 days before the research; The man patients who must agree to take contraceptive methods during the research and within another 8 weeks after it.
Exclusion Criteria:
- Histological or cytological confirmation of mucinous adenocarcinoma or ovarian transcoelomic metastasis
- Patients who had previously received treatment with Anlotinib or anti-programmed cell death protein 1 (PD-1), programmed cell death protein 1 ligand 1 (PD-L1), or cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) inhibitors other immunotherapy against .
- Patients who had previously received treatment within 2 weeks or Participated in other anti-tumor clinical trials within 4 weeks.
- Patients with a large amount of pleural effusion or ascites requiring drainage.
- Has known active central nervous system (CNS) metastases and/or carcinomatous meningitis.
- Has a known additional malignancy that is progressing or requires active treatment. Exceptions include basal cell carcinoma of the skin, squamous cell carcinoma of the skin, or in situ cervical cancer that has undergone potentially curative therapy.
- Patients who underwent major surgery within 4 weeks.
- Regardless of the severity, patients with any physical signs or history of bleeding, patients with bleeding or bleeding events greater than or equal to CTCAE 3 within four weeks prior to the first administration, or patients with unhealed wounds, fractures, ulcers.
- Patients with a risk of gastrointestinal bleeding may not be enrolled.
- Patients with arterial or venous thromboembolic events occurred within 6 months, such as cerebrovascular accident (including transient ischemic attack), deep vein thrombosis and pulmonary embolism.
- Patients with any severe and/or unable to control diseases,including: Patients with unsatisfactory blood pressure control using antihypertensive drugs (systolic blood pressure ≥150 mmHg or diastolic blood pressure ≥100) mmHg); Patients with Grade 2 or higher myocardial ischemia, myocardial infarction or malignant arrhythmias(including male QTc≥450ms; female QTc≥470ms) and patients with Grade 2 or higher congestive heart failure (NYHA Classification); Patients with active or unable to control serious infections, which is over level 2 in CTC AE (4.0); Patients with poorly controlled diabetes (fasting blood glucose(FBG)>10mmol/L); Patients with kidney failure who require hemodialysis or peritoneal dialysis; Patients with interstitial lung disease with symptoms or signs of activity;Patients with a history of immunodeficiency, including a positive HIV test or other acquired, congenital immunodeficiency disease, or a history of organ transplantation; Urine routine indicates that urine protein ≥ ++, and confirmed 24-hour urine protein quantitation > 1.0 g; Patients with any of the following coagulation functions are abnormal, including: Prothrombin time (PT)>ULN+4s, Activated partial thromboplastin time (APTT) >1.5ULN s, international normalized ratio (INR)>1.5; Patients with a seizure disorder who require pharmacotherapy.
- Patients who have got non remissive toxic reactions derived from any treatment, which is over level 1 in CTC AE (4.0).
- Has a diagnosis of immunodeficiency or is receiving chronic steroid therapy of prednisone ≥ 10 mg daily or any equivalent dose of corticosteroids.
- Has received a live vaccine or attenuated vaccine within 30 days prior to trial registration.
- Symptoms that affect oral medication and cannot be controlled through proper treatment (such as inability to swallow, chronic diarrhoea and intestinal obstruction, etc.).
- Female patients who are pregnant or breastfeeding.
- Patients with drug abuse history and unable to get rid of or patients with mental disorders.
- Patients who had serious adverse effect to Anlotinib or Penpulimab or any of its excipients
- Known hypersensitivity to other Monoclonal Antibody or any of its excipients.
- Patients with concomitant diseases which could seriously endanger their own safety or could affect completion of the study according to investigators' judgment.
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: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Anlotinib+Penpulimab
|
Penpulimab 200 mg administered intravenously every 3 weeks.
Other Names:
12mg, continuous oral 2 weeks stop for 1 week, 21 days for a treatment cycle.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Progression-free survival (PFS)
Time Frame: up to 24 months
|
Progression-free Survival (PFS) (median) was determined using the number of months measured from the initial date of treatment to the date of documented progression, or the date of death (in the absence of progression) of participants.
Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.1), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions.
|
up to 24 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Disease Control Rate (DCR)
Time Frame: up to 24 months
|
Disease control rate is defined as the percentage of subjects whose best response was CR, PR or stable disease (SD) according to the RECIST v1.1.
|
up to 24 months
|
Objective Response Rate (ORR)
Time Frame: up to 24 months
|
Objective response rate is defined as the percentage of subjects whose best response was complete response (CR) or partial response (PR) according to the RECIST v1.1
|
up to 24 months
|
Duration of Response (DOR)
Time Frame: up to 24 months
|
Duration of Response is defined as the percentage of subjects whose best response was CR, PR or stable disease (SD) according to the RECIST v1.1 or death due to any cause, whichever occurs first.
|
up to 24 months
|
Number of participants with treatment-related adverse events as assessed by CTCAE v5.0
Time Frame: Until 30 day safety follow-up visit
|
Adverse events assessed using the National Cancer Institute Common Terminology Criteria for Adverse Events (version 5.0).
|
Until 30 day safety follow-up visit
|
Overall Survival (OS)
Time Frame: Up to 24 months
|
Overall Survival (OS) (median) is determined using the number of months measured from the initial date of treatment to the recorded date of death of participants.
|
Up to 24 months
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of TB cells count and interleukin-6/8/10
Time Frame: through study completion, an average of 2 year
|
Objectives to analyse the subsets of TB cells and interleukin-6/8/10 associated treatment.
|
through study completion, an average of 2 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Jianfeng Zhou, Peking Union Medical College Hospital
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)
November 5, 2021
Primary Completion (Anticipated)
August 23, 2022
Study Completion (Anticipated)
August 23, 2023
Study Registration Dates
First Submitted
July 5, 2021
First Submitted That Met QC Criteria
July 13, 2021
First Posted (Actual)
July 21, 2021
Study Record Updates
Last Update Posted (Actual)
March 8, 2022
Last Update Submitted That Met QC Criteria
March 6, 2022
Last Verified
March 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HS-2986B
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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.
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