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Clinical trial · no report yet · Phase 3
LIMBER-304 trial: what clinicians have said so far
To Evaluate Efficacy and Safety of Parsaclisib and Ruxolitinib in Participants With Myelofibrosis Who Have Suboptimal Response to Ruxolitinib (LIMBER-304)
- NCT04551053 ↗
- Terminated
- Incyte Corporation
- Focused size, estimated: 1–150 verified statements
We haven't built an HCP commentary report on LIMBER-304 (parsaclisib plus ruxolitinib in myelofibrosis with suboptimal response to ruxolitinib) yet. This page shows the registry record and the public commentary we found that names the trial. A report reads that commentary and sets out what clinicians said about the trial, each point linked to its source. How reports are made.
Indexed commentary on LIMBER-304 so far
Podcasts, YouTube videos and X posts we have indexed that name the trial. It is where a report starts, not where it ends: the build searches for more, so finished reports usually cover more than this.
| Indexed so far | |
|---|---|
| 4 posts on X |
The trial
ClinicalTrials.gov- Official title
- A Randomized, Double-Blind, Placebo-Controlled Study of the PI3Kδ Inhibitor Parsaclisib Plus Ruxolitinib in Participants With Myelofibrosis Who Have Suboptimal Response to Ruxolitinib
- Phase
- Phase 3
- Status
- Terminated
- Conditions
- Myelofibrosis; Primary Myelofibrosis; Post Essential Thrombocythemia Myelofibrosis; Post Polycythemia Vera Myelofibrosis
- Interventions
- parsaclisib; ruxolitinib; placebo
- Arms
- Group A : ruxolitinib +parsaclisib · Experimental
- Group B : ruxolitinib + placebo · Placebo comparator
- Enrollment
- 177
- Primary outcomes
- Percentage of Participants Achieving ≥25% Reduction in Spleen Volume From Baseline to Week 24 as Measured by Magnetic Resonance Imaging (MRI) (or Computed Tomography [CT] Scan in Applicable Participants)
- Sponsor
- Incyte Corporation
- Start
- May 26, 2021
- Primary completion
- Aug 16, 2023
- Results posted
- Yes
- Registry record
- NCT04551053 · updated Oct 2, 2025