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NCT04524195
PET Imaging With [18F]F-AraG in Advanced Non-small Cell Lung Cancer (NSCLC)
Phase 1 trial testing [18F]F-AraG Injection in Non-small Cell Lung Cancer (NSCLC) in 4 participants. Terminated before completion.
27 November 2023
Quick facts
| Lead sponsor | Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins |
|---|---|
| Phase | Phase 1 |
| Status | Terminated |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | diagnostic |
| Enrollment | 4 |
| Start date | 1 February 2021 |
| Primary completion | 27 November 2023 |
| Estimated completion | 27 November 2023 |
| Sites | 1 location across United States |
Drugs / interventions tested
- [18F]F-AraG Injection — full drug profile →
Conditions studied
- Non-small Cell Lung Cancer (NSCLC) — all drugs for Non-small Cell Lung Cancer (NSCLC) →
Sponsor
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins — full company profile →
Who can join
18 and older, any sex, with Non-small Cell Lung Cancer (NSCLC). Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This is a prospective, single center, single-arm clinical trial in 20 patients with non-small cell lung cancer (NSCLC) undergoing PD-1/PD-L1-directed therapy. This research is being done to find out if the radioactive compound called \[18F\]F-AraG is a helpful imaging agent for detecting changes in cancer's anti-tumor immune response (or activation of T-cell) levels for non-small cell lung cancer (NSCLC) patients who will receive a cancer immunotherapy regimen (immunotherapy works by encouraging the body's own immune system to attack the cancer cells).
Publications & conference data
4 peer-reviewed publications reference this trial (live from Europe PMC):
-
Molecular Immune Targeted Imaging of Tumor Microenvironment.
Rakhshandehroo T, Smith BR, Glockner HJ, Rashidian M, et al · · 2022 · cited 19× · PMID 35223381 · DOI 10.7150/ntno.66556 -
Clinical Application of ImmunoPET Targeting Checkpoint Inhibitors.
Abenavoli EM, Linguanti F, Calabretta R, Delgado Bolton RC, et al · · 2023 · cited 11× · PMID 38067379 · DOI 10.3390/cancers15235675 -
Advancing In Vivo Detection of T-Cell Function: Development and Preclinical Evaluation of <sup>89</sup>Zr-Ivuxolimab, a Human OX40 PET Tracer.
Kalita M, Kuo RC, Reyes ST, Colburg DRC, et al · · 2025 · cited 1× · PMID 40707142 · DOI 10.2967/jnumed.125.269799 -
Metabolic [¹⁸F]F-AraG PET imaging of T Cell activation: a functional complement to cell-specific immune tracers.
Almutairi WM, Gopaulchan M, Bhaskara R, Zheng QH, et al · · 2026 · PMID 42001384 · DOI 10.1186/s13550-026-01436-6
Verify or expand the search:
- PubMed search for NCT04524195
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Non-small Cell Lung Cancer (NSCLC)
Currently open trials in the same condition.
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Other Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins trials
Trials by the same sponsor.
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- NCT07140315 — DK222 Study at Hopkins · Phase 1 · recruiting
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04524195 (US National Library of Medicine, public domain)
- 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 Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
- Last refreshed: 17 January 2024
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/NCT04524195.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing