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NCT05462873TerminatedPhase 1

A Study to Investigate the Safety and Tolerability of Intravenous QEQ278 in Patients With Advanced Solid Tumors

A Phase I/Ib, Open-label, Multi-center, Study of QEQ278 in Patients With Advanced Solid Tumors

Source: ClinicalTrials.gov · Last updated 17 Feb 2026

Reason given: Business decision and not related to safety concerns

Brief summary (registry, in English)

To characterize safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary anti-tumor activity of QEQ278 in adult patients with advanced/metastatic non-small cell lung cancer, esophageal squamous cell carcinoma, renal cell carcinoma, and human papilloma virus associated head and neck squamous cell carcinoma.

Status (registry)
Terminated
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
30 (actual)
First submitted
14 Jul 2022
Start date
4 Apr 2023
Primary completion date
26 Jan 2026
Lead sponsor
Novartis Pharmaceuticals
NCT number
NCT05462873

Who cannot take part

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

Prior treatment

  • Active previously documented or suspected autoimmune disease. Patients with vitiligo, type I diabetes, residual hypothyroidism only requiring hormone replacement, psoriasis not requiring systemic treatment, or conditions not expected to recur should not be excluded. Patients previously exposed to anti-PD-1/PD-L1 treatment who are adequately treated for skin rash or with replacement therapy for endocrinopathies should not be excluded.
  • Patients who discontinued prior anti-PD-1 therapy due to an anti-PD-1-related toxicity

Other illness

  • Patients with a history of or current interstitial lung disease or pneumonitis ≥ Grade 2.
  • Clinically significant cardiac disease or risk factors at screening
  • Infections:
  • Known history of testing positive for Human Immunodeficiency Virus infection.
  • Active Hepatitis B and / or Hepatitis C.
  • Active, documented COVID-19 infection
  • Known history of tuberculosis
  • Any serious uncontrolled infection (acute or chronic).
  • Systemic chronic steroid therapy (>10 mg/day prednisone or equivalent) or any immunosuppressive therapy, other than replacement-dose steroids in the setting of adrenal insufficiency, within 7 days of the first dose of study treatment. Topical, inhaled, and ophthalmic steroids are allowed.
    • Other protocol-defined inclusion/exclusion criteria may apply.

Other

  • Insufficient bone marrow function at screening:

Who the study is looking for

  • Signed informed consent must be obtained prior to participation in the study.
  • Adult men and women ≥ 18 years of age.
  • Histologically confirmed and documented advanced malignancies (locally advanced malignancies, non-curable by surgery or radiotherapy and metastatic disease). Disease must be measurable, including presence of at least one measurable lesion, as determined by RECIST v1.1.
  • In the opinion of the treating investigator, patients must have received, but are not benefitting from standard therapies, be intolerant or ineligible to receive such therapy, or have no standard therapy option for the respective disease types (diseases listed below), as well as any other therapies deemed to be standard by local/institutional standard.
  • Non-small cell lung cancer
  • Esophageal squamous cell carcinoma
  • Renal cell carcinoma
  • HPV-associated head and neck squamous cell carcinoma
  • Must have a site of disease amenable to biopsy and be a candidate for tumor biopsy according to the treating institution's guidelines. The patient must be willing to undergo a new tumor biopsy at screening and during treatment.

Age in the registry: 18 years to 100 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (12)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
-BrusselsBelgiumUnknown status
-EssenGermanyUnknown status
-BarcelonaSpainUnknown status
-ParisFranceUnknown status
-MilanItalyUnknown status
-KashiwaJapanUnknown status
-SingaporeSingaporeUnknown status
-TaipeiTaiwanUnknown status
Massachusetts General HospitalBostonUnited StatesUnknown status
Massachusetts General Hospital Dept. of Mass General HospitalBostonUnited StatesUnknown status
Florida Cancer SpecialistsFort MyersUnited StatesUnknown status
University of California LALos AngelesUnited StatesUnknown status

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