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NCT06409429Not yet recruitingPhase 2/3

Nimotuzumab Combined With GX as Postoperative Adjuvant Therapy in Pancreatic Cancer

A Prospective, Multicenter, Randomized, Double-blind, Placebo-controlled Study of Nimotuzumab Combined With GX as Postoperative Adjuvant Therapy in Pancreatic Cancer

Source: ClinicalTrials.gov · Last updated 10 May 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This is a prospective, multicenter, randomized, double-blind, placebo-controlled study. The main purpose of the study is to evaluate the clinical efficacy and safety of Nimotuzumab combined with GX for postoperative adjuvant treatment of pancreatic cancer.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 2/3
Study type
Interventional
Enrollment
146 (estimated)
First submitted
7 May 2024
Start date
May 2024
Primary completion date
May 2027
Lead sponsor
Tianjin Medical University Cancer Institute and Hospital
NCT number
NCT06409429

What you commit to

  • Study type: Interventional · Phase 2/3
  • Planned participants: 146
  • From May 2024 to the primary completion date, May 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • 1\. Prior neo-adjuvant treatment, radiation therapy, or systemic therapy for pancreatic adenocarcinoma;
  • 2\. Accompanied by other serious diseases, including but not limited to: active infections; unmanageable diabetes mellitus and uncontrolled hypertension (SBP\>160mmHg or DBP\>100mmHg); compensatory heart failure (NYHA grade III and IV), unstable angina or poorly controlled arrhythmias within 3 months prior to randomization; presence of uncontrolled pleural effusion, pericardial effusion, or ascites requiring drainage; severe portal hypertension; gastric outlet obstruction; Respiratory insufficiency and Severe lung disease; Central Nervous System Disease or mental illness;
  • 7\. Factors that significantly affect oral drug absorption, such as dysphagia, chronic diarrhea, gastrointestinal obstruction, etc;

Other illness

  • 3\. History of other malignancies (except cured basal cell carcinoma of the skin and carcinoma in situ of the cervix);
  • 4\. bleeding or clotting disorder;
  • 5.Postoperative complications such as bleeding, pancreatic fistula, gastric obstruction, abdominal infection, and biliary fistula, which made the patient unable to receive adjuvant therapy within 12 weeks after surgery;
  • 6\. Known allergy to prescription or any component of the prescription used in this study;
  • 8\. Known HIV, or syphilis infection, or active hepatitis (hepatitis B, hepatitis C);

Other

  • 9.Other reasons that are not suitable to participate in this study according to the researcher's judgment

Who the study is looking for

  • 1\. Able and willing to provide a written informed consent.
  • 2\. Age 18-75 years old, gender unlimited;
  • 3\. Histologically or cytologically confirmed resected pancreatic ductal adenocarcinoma (PDAC), resectable evaluation is based on criteria of NCCN guidelines, no evidence of distant metastasis as demonstrated by imaging;
  • 4\. Postoperative pathology suggested R0/R1 resection;
  • 5\. Adequate organ and bone marrow function, defined as follows: absolute neutrophil count (ANC)≥1.5×10\^9/L; platelets≥100×10\^9/L; hemoglobin≥9.0 g/dL; serum total bilirubin (TBIL)≤1.5×ULN; aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 times the upper limit of normal (ULN); serum creatinine≤1.5×ULN or estimated creatinine clearance \> 60 mL/min;
  • 6\. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1;
  • 7\. Postoperative survival is expected to be ≥3 months;
  • 8\. Fertile subjects are willing to take contraceptive measures during the study period.

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Tianjin Medical University Cancer Institute and Hospital
Coordinator of this site? Confirm its status
TianjinChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.