Skip to content

H1-antihistaminE treatment in combiNation with immunotHerapy in pAtieNts with advanced non small cell lung canCEr: A single- center phase II trial-ENHANCE

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-518633-28-00
Acronym
ENHANCE
Enrollment
9
Registered
2024-12-10
Start date
2022-10-13
Completion date
Unknown
Last updated
2024-12-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Advanced non small lung cancer

Brief summary

Objective response rate according to RECIST 1.1., ORR; defined as complete or partial response at any timepoint during study period.

Detailed description

Secondary Endpoint: Progression-free survival (PFS), Overall survival (OS). Exploratory Endpoint: Safety & tolerability of fexofenadine in terms of haematologic and nonhaematologic side effects as assessed by the investigators. Quality of life (QoL) with focus on sleeping behavior in patients receiving fexofenadine assessed by the Pittsburgh Sleep Quality Index (PSQI), EORTC QLQ-c30 questionnaire and Lung Cancer Symptom Scale (LCSS). Analysis of predictive factors for the enhancement of immunoth

Interventions

DRUGAllegra 120 mg Filmtabletten

Sponsors

Medical University Of Vienna
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Objective response rate according to RECIST 1.1., ORR; defined as complete or partial response at any timepoint during study period.

Secondary

MeasureTime frame
Secondary Endpoint: Progression-free survival (PFS), Overall survival (OS). Exploratory Endpoint: Safety & tolerability of fexofenadine in terms of haematologic and nonhaematologic side effects as assessed by the investigators. Quality of life (QoL) with focus on sleeping behavior in patients receiving fexofenadine assessed by the Pittsburgh Sleep Quality Index (PSQI), EORTC QLQ-c30 questionnaire and Lung Cancer Symptom Scale (LCSS). Analysis of predictive factors for the enhancement of immunoth

Countries

Austria

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026