18 and older, any sex, with Non-small Cell Lung Cancer. Patients with the condition only — healthy volunteers not accepted.
Results — posted to ClinicalTrials.gov
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
Molecularly-informed Treatment RecommendationsPrimary· Measured up to 12 weeks from randomization
Receipt of a molecularly-informed treatment recommendation for patients with metastatic NSq NSCLC at the time of the patient's initial oncology visit.
Group
Value
95% CI
Telehealth
2
Usual Care
2
Rate of Telehealth Visit CompletionSecondary· Measured up to 3 weeks from randomization
Telehealth visit completion defined as successful completion of a telehealth visit prior to biopsy
Group
Value
95% CI
Telehealth
25
Rate of Completion of Comprehensive Molecular Testing (Tissue and/or Plasma Testing) Prior to Initiation of First Line TherapySecondary· Measured up to 12 weeks from randomization
Rate of completion of comprehensive molecular testing (tissue and/or plasma testing) prior to initiation of first line therapy
Group
Value
95% CI
Telehealth
26
Usual Care
12
Identification of One or More Targetable MutationsSecondary· Measured up to 12 weeks from randomization
Identification of one or more targetable mutations
Group
Value
95% CI
Telehealth
2
Usual Care
2
Timeliness of Molecularly-informed Treatment RecommendationSecondary· Measured up to 12 weeks from randomization
Time from randomization to recommendation of a molecularly-informed treatment, as documented in the EMR
Group
Value
95% CI
Telehealth
17.6
16 – 18
Usual Care
38.5
27.5 – 43
Overall SurvivalSecondary· Measured up to 1 year from the time of randomization to death from any cause
Overall survival
Group
Value
95% CI
Telehealth
5
Usual Care
4
Telehealth
1
Usual Care
2
Proportion of Patients With Diagnosis Other Than Metastatic Nonsquamous NSCLC (Telehealth Arm Only)Secondary· Measured at 12 weeks from randomization
Proportion of patients with diagnosis other than metastatic nonsquamous NSCLC (Telehealth arm only)
Group
Value
95% CI
Telehealth
21
Time From Randomization to Treatment InitiationSecondary· Measured at 12 weeks from randomization
Time from randomization to treatment initiation
Group
Value
95% CI
Telehealth
27.6
23 – 35
Usual Care
50.3
38 – 67
Sponsor's own description
The goal of this trial is to design and test a telehealth nurse navigation intervention for patients with suspected locally advanced/metastatic NSCLC to improve timely molecularly-informed treatment recommendations through early integration of concurrent molecular testing.
Publications & conference data
3 peer-reviewed publications reference this trial (live from Europe PMC):
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Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by Abramson Cancer Center at Penn Medicine
Last refreshed: 22 April 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05790460.