Anlotinib Plus Penpulimab (AK105) for Chemo-refractory Metastatic Colorectal Cancer:ALTER-C003

NCT04970914 | Unknown Phase 2

• 1 other identifier: HS-2986B
• Study Type: interventional
• Target: 32
• Locations: 1 country
• Sites: 8

Brief Summary

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)

Conditions

Colorectal Cancer

Outcome Measures

Primary Outcomes (1)

• Progression-free survival (PFS)

  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 Outcomes (5)

• Objective Response Rate (ORR)

  up to 24 months

• Disease Control Rate (DCR)

  up to 24 months

• Duration of Response (DOR)

  up to 24 months

• Number of participants with treatment-related adverse events as assessed by CTCAE v5.0

  Until 30 day safety follow-up visit

• Overall Survival (OS)

  Up to 24 months

Other Outcomes (1)

• Number of TB cells count and interleukin-6/8/10

  through study completion, an average of 2 year

Study Arms (1)

Anlotinib+Penpulimab

EXPERIMENTAL

Drug: Anlotinib; Drug: Penpulimab

Interventions

Anlotinib DRUG

12mg, continuous oral 2 weeks stop for 1 week, 21 days for a treatment cycle.

Also known as: anlotinib hydrochloride

Anlotinib+Penpulimab

Penpulimab DRUG

Penpulimab 200 mg administered intravenously every 3 weeks.

Also known as: AK105

Anlotinib+Penpulimab

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• 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.

You may not qualify if:

• 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.).

Sponsors & Collaborators

• Peking Union Medical College Hospital: lead

Study Sites (8)

Beijing Tiantan Hospital, Capital Medical University

Beijing, Beijing Municipality, China

RECRUITING

China-Japan friendship hospital

Beijing, Beijing Municipality, China

NOT YET RECRUITING

Hebei Petro China Central Hospital

Langfang, Hebei, China

NOT YET RECRUITING

The Fourth Hospital of Hebei Medical University (Hebei Cancer Hospital)

Shijiazhuang, Hebei, China

NOT YET RECRUITING

General Hospital of Tianjin Medical University

Tianjin, Tianjin Municipality, China

RECRUITING

Peking Union Medical College Hospital

Beijing, China

RECRUITING

The First Hospital Of China Medical University

Shenyang, China

NOT YET RECRUITING

The People's Hospital Of Liaoning Province

Shenyang, China

NOT YET RECRUITING

MeSH Terms

Conditions

Colorectal Neoplasms

Interventions

anlotinib; penpulimab

Condition Hierarchy (Ancestors)

Intestinal Neoplasms; Gastrointestinal Neoplasms; Digestive System Neoplasms; Neoplasms by Site; Neoplasms; Digestive System Diseases; Gastrointestinal Diseases; Colonic Diseases; Intestinal Diseases; Rectal Diseases

Study Officials

• Jianfeng Zhou

  Peking Union Medical College Hospital

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Jianfeng Zhou

CONTACT

011-86-10-69156114; ZhouJF@pumch.cn

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Prof.M.D.

Study Record Dates

• First Submitted: July 5, 2021
• First Posted: July 21, 2021
• Study Start: November 5, 2021
• Primary Completion: August 23, 2022
• Study Completion: August 23, 2023
• Last Updated: March 8, 2022

Record last verified: 2022-03

Data Sharing

• IPD Sharing: Will not share

Locations

CN (8)