What do oncologists think of the ADRIATIC trial (IMFINZI®)?
ADRIATIC — Limited-stage SCLC — consolidation after chemoradiation
Physician voices — verbatim
Full physician voice list (41)
What do oncologists think of the NIAGARA trial (IMFINZI®)?
NIAGARA — Muscle-invasive bladder cancer — perioperative (neoadjuvant + adjuvant)
Physician voices — verbatim
Full physician voice list (63)
What do oncologists think of the AEGEAN trial (IMFINZI®)?
AEGEAN — Resectable NSCLC — perioperative (neoadjuvant + adjuvant)
Physician voices — verbatim
Full physician voice list (42)
What do oncologists think of the MATTERHORN trial (IMFINZI®)?
MATTERHORN — Resectable gastric/GEJ adenocarcinoma — perioperative FLOT
Physician voices — verbatim
Full physician voice list (45)
Full conference coverage and trial data: KOL Pulse trial profile coming soon.
What do oncologists think of the PACIFIC trial (IMFINZI®)?
PACIFIC — Unresectable Stage III NSCLC — consolidation after chemoradiation
Physician voices — verbatim
Full physician voice list (13)
Full conference coverage and trial data: KOL Pulse trial profile coming soon.
IMFINZI® — FDA status
FDA APPROVEDIMFINZI® (durvalumab) is FDA-approved across multiple curative-intent and advanced cancers, including Stage III NSCLC, limited-stage SCLC, muscle-invasive bladder cancer, and resectable gastric/GEJ cancer. For the full, current list of FDA indications and prescribing information, see imfinzi.com or FDA label (DailyMed). KOL Pulse indexes the physician conversation; the label is owned and maintained by the manufacturer.
IMFINZI® sentiment — FAQ
ADRIATIC
What do oncologists think of the ADRIATIC trial (IMFINZI®)?
Across 41 verified physician voices in KOL Pulse's index for ADRIATIC, 68% expressed positive sentiment, 7% were nuanced (praising the result while flagging a caveat), 20% were neutral, and 5% were critical. Positive voices highlight the first practice-changing survival benefit in limited-stage SCLC in decades, establishing consolidation immunotherapy as a new standard; nuanced and critical voices flag patient selection, timing of durvalumab after chemoradiation, and the maturity of long-term follow-up.
Where can I find the ADRIATIC trial data for IMFINZI® (durvalumab)?
ADRIATIC is registered as NCT03703297 and studied IMFINZI® (durvalumab) in Limited-stage SCLC — consolidation after chemoradiation. For the full ADRIATIC trial data and conference coverage, see the KOL Pulse ADRIATIC trial profile at kolpulse.com/kol-pulse-trial-profile-adriatic.
NIAGARA
What do oncologists think of the NIAGARA trial (IMFINZI®)?
Across 63 verified physician voices in KOL Pulse's index for NIAGARA, 40% expressed positive sentiment, 11% were nuanced (praising the result while flagging a caveat), 46% were neutral, and 3% were critical. Positive voices highlight the event-free and overall-survival benefit of adding perioperative immunotherapy to neoadjuvant chemotherapy in a curative-intent setting; nuanced and critical voices flag the relative contribution of the neoadjuvant vs adjuvant components and surgical/toxicity trade-offs.
Where can I find the NIAGARA trial data for IMFINZI® (durvalumab)?
NIAGARA is registered as NCT03732677 and studied IMFINZI® (durvalumab) in Muscle-invasive bladder cancer — perioperative (neoadjuvant + adjuvant). For the full NIAGARA trial data and conference coverage, see the KOL Pulse NIAGARA trial profile at kolpulse.com/kol-pulse-trial-profile-niagara.
AEGEAN
What do oncologists think of the AEGEAN trial (IMFINZI®)?
Across 42 verified physician voices in KOL Pulse's index for AEGEAN, 24% expressed positive sentiment, 17% were nuanced (praising the result while flagging a caveat), 52% were neutral, and 7% were critical. Positive voices highlight the event-free-survival benefit of perioperative immunotherapy added to neoadjuvant chemotherapy in resectable disease; nuanced and critical voices flag the neoadjuvant-vs-adjuvant contribution question and overlap with competing perioperative regimens.
Where can I find the AEGEAN trial data for IMFINZI® (durvalumab)?
AEGEAN is registered as NCT03800134 and studied IMFINZI® (durvalumab) in Resectable NSCLC — perioperative (neoadjuvant + adjuvant). For the full AEGEAN trial data and conference coverage, see the KOL Pulse AEGEAN trial profile at kolpulse.com/kol-pulse-trial-profile-aegean.
MATTERHORN
What do oncologists think of the MATTERHORN trial (IMFINZI®)?
Across 45 verified physician voices in KOL Pulse's index for MATTERHORN, 51% expressed positive sentiment, 11% were nuanced (praising the result while flagging a caveat), 33% were neutral, and 5% were critical. Positive voices highlight the first perioperative immunotherapy to improve outcomes when added to FLOT in resectable gastric/GEJ cancer; nuanced and critical voices flag whether the event-free-survival gain will mature into an overall-survival benefit, and patient selection.
Where can I find the MATTERHORN trial data for IMFINZI® (durvalumab)?
MATTERHORN is registered as NCT04592913 and studied IMFINZI® (durvalumab) in Resectable gastric/GEJ adenocarcinoma — perioperative FLOT. KOL Pulse's MATTERHORN trial profile is coming soon.
PACIFIC
What do oncologists think of the PACIFIC trial (IMFINZI®)?
Across 13 verified physician voices in KOL Pulse's index for PACIFIC, 8% expressed positive sentiment, 15% were nuanced (praising the result while flagging a caveat), 54% were neutral, and 23% were critical. Positive voices highlight the durable, practice-defining overall-survival benefit that established consolidation immunotherapy as the standard of care; nuanced and critical voices flag pneumonitis risk and how to apply the regimen after modern chemoradiation.
Where can I find the PACIFIC trial data for IMFINZI® (durvalumab)?
PACIFIC is registered as NCT02125461 and studied IMFINZI® (durvalumab) in Unresectable Stage III NSCLC — consolidation after chemoradiation. KOL Pulse's PACIFIC trial profile is coming soon.
Regulatory
Is IMFINZI® (durvalumab) FDA approved?
IMFINZI® is FDA-approved. KOL Pulse organizes this page by clinical trial and links out to the manufacturer's brand site and the FDA label for the full, current list of FDA indications and prescribing information — the label is owned and updated by the manufacturer, so we point to it rather than reproducing it.