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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

Full criteria on ClinicalTrials.gov

Sites (11)

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

SiteCityCountrySite status
NeoTX - 10308
Coordinator of this site? Confirm its status
AustinUnited StatesUnknown status
NeoTX - 10309
Coordinator of this site? Confirm its status
DallasUnited StatesUnknown status
NeoTX - 10307
Coordinator of this site? Confirm its status
DaphneUnited StatesUnknown status
NeoTX - 10312
Coordinator of this site? Confirm its status
El PasoUnited StatesUnknown status
NeoTX - 10311
Coordinator of this site? Confirm its status
FairfaxUnited StatesUnknown status
NeoTX - 10306
Coordinator of this site? Confirm its status
Lone TreeUnited StatesUnknown status
NeoTX - 10304
Coordinator of this site? Confirm its status
MinneapolisUnited StatesUnknown status
NeoTX - 10100
Coordinator of this site? Confirm its status
MorristownUnited StatesUnknown status
NeoTX - 10302
Coordinator of this site? Confirm its status
ScottsdaleUnited StatesUnknown status
NeoTX - 10303
Coordinator of this site? Confirm its status
TucsonUnited StatesUnknown status
NeoTX - 10310
Coordinator of this site? Confirm its status
TylerUnited StatesUnknown status

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