Expert Interview
A Second Look: Discussing the Phase 3 LELANTOS data of FibroGen's Pamrevlumab in patients with non-ambulatory DMD
Ticker(s): FGENInstitution: Texas Children's Hospital / Baylor College of Medicine
- Assistant Professor of Pediatric Neurology at Baylor College of Medicine.
- Manages 36 patients with SMA and 85 patients with DMD per year.
- PI on several clinical trials including the pamrevlumab study; Clinical and research interest in muscular dystrophy with focus on Duchenne Muscular Dystrophy.
What are your high level thoughts, including familiarity with this program even before we approached you with this topic?
Added By: sara_adminWhat are personal thoughts on targeting CTGF as just a
general idea in DMD? Are you more optimistic or pessimistic about this pathway making a big
difference in these patients?
Could you talk about the natural history of DMD? For the 46 patients in the placebo
arm what your expectation would be after 104 weeks, what kind of FVC decline
would you expect, and is there even a possibility that the placebo arm would be
stable?
Looking at upper limb performance, do you think that
those all correlate together, or what's the chance that we might get a split
result where there's really encouraging signs on one endpoint, but then on the
others maybe not so much?
If this drug did nothing else but stabilize the functional assessment, even
if we don't know the effect size, would that be pretty likely to yield a positive
outcome?
What is your level of confidence regarding the ambulatory trial, and is the North Star Ambulatory Assessment endpoint more difficult to hit as compared to the non-ambulatory trial
endpoint?
Are You Interested In These Questions?
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