NCT04880863CompletedPhase 2
NAP in Combination With Docetaxel Following Obinutuzumab Pretreatment in Subjects With Checkpoint Inhibitor Pretreated Advanced or Metastatic NSCLC
Phase 2a Open-Label, Multicenter Trial of Naptumomab Estafenatox (NAP) in Combination With Docetaxel Following Obinutuzumab Pretreatment in Subjects With Checkpoint Inhibitor Pretreated Advanced or Metastatic Non-Small Cell Lung Cancer
Source: ClinicalTrials.gov · Last updated 3 Mar 2025
Brief summary (registry, in English)
Phase 2a Open-Label, Multicenter Trial of Naptumomab Estafenatox (NAP), following Obinutuzumab Pretreatment, on Days -13 and -12. NAP will be administered on Days 1-4 of treatment cycles 1-6, followed by docetaxel on Day 5. Starting cycle 7, NAP at a higher dose will be administered on Day 1 only and docetaxel on Day 2, in 21 days treatment cycles. When NAP is administered as monotherapy and not earlier than cycle 7, NAP will be administered on Day 1 only and cycles will be of 28 days treatment cycle.
- Status (registry)
- Completed
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 38 (actual)
- First submitted
- 3 May 2021
- Start date
- Oct 2021
- Primary completion date
- Jan 2024
- Lead sponsor
- NeoTX Therapeutics Ltd.
- Diseases
- Lung cancer
- NCT number
- NCT04880863
What you commit to
- Study type: Interventional · Phase 2
- Participants enrolled: 38
- From Oct 2021 to the primary completion date, Jan 2024
- 11 sites 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.
Criteria the registry did not label
- Main Inclusion Criteria:
- Subjects must be at least 18 years of age
- Subjects must have histologically and/or cytologically confirmed NSCLC
- Subjects must have incurable (advanced or metastatic) disease at the time of enrolment
- Subjects must have an Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1
- Subjects must provide signed informed consent prior to any study specific procedures that are not part of standard medical care.
- Subjects must have measurable neoplastic disease based on the iRECIST criteria
- Subjects must have received as least 1 and no more than 2 prior systemic regimens for the treatment of advanced/metastatic NSCLC. Patients are required to have progressed following treatment with both platinum-based chemotherapy and an anti-PD-(L)1 antibody administered either sequentially or concurrently. A prior PD-1/PD-L1 inhibitor is, however, not required if there was prior exposure to targeted therapies for a driver mutation positive tumors (e.g. EGFR or ALK inhibitors).
- Main Exclusion Criteria:
- Subjects with active infection requiring treatment within 3 days of C1D1.
- Subjects with other active neoplastic disease requiring concurrent anti-neoplastic treatment
- Subjects with known, suspected or documented parenchymal brain metastases unless treated with surgery and/or radiation, with the subject neurologically stable and off pharmacologic doses of systemic glucocorticoids; subjects with leptomeningeal metastases are not eligible. Patients should have completed brain radiation for at least 14 days and be off steroids.
- Active or previously documented autoimmune or inflammatory disorders such as, but not limited to rheumatoid arthritis, systemic lupus erythematosus, uveitis, ulcerative colitis, Crohn's syndrome, Wegener's syndrome, multiple sclerosis, myasthenia gravis, scleroderma and sarcoidosis. The following are exceptions to this criterion:
- Vitiligo or psoriasis not requiring systemic treatment (within the last 2 years)
- Subjects with endocrinopathies (e.g. following Hashimoto syndrome) stable on hormone replacement or do not require any therapy.
- History of primary immunodeficiency
- Subjects with a history or prior allogeneic organ transplant
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (11)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| NeoTX - 10308 Coordinator of this site? Confirm its status | Austin | United States | Unknown status |
| NeoTX - 10309 Coordinator of this site? Confirm its status | Dallas | United States | Unknown status |
| NeoTX - 10307 Coordinator of this site? Confirm its status | Daphne | United States | Unknown status |
| NeoTX - 10312 Coordinator of this site? Confirm its status | El Paso | United States | Unknown status |
| NeoTX - 10311 Coordinator of this site? Confirm its status | Fairfax | United States | Unknown status |
| NeoTX - 10306 Coordinator of this site? Confirm its status | Lone Tree | United States | Unknown status |
| NeoTX - 10304 Coordinator of this site? Confirm its status | Minneapolis | United States | Unknown status |
| NeoTX - 10100 Coordinator of this site? Confirm its status | Morristown | United States | Unknown status |
| NeoTX - 10302 Coordinator of this site? Confirm its status | Scottsdale | United States | Unknown status |
| NeoTX - 10303 Coordinator of this site? Confirm its status | Tucson | United States | Unknown status |
| NeoTX - 10310 Coordinator of this site? Confirm its status | Tyler | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.