will joining the this program provide and for to financial afternoon development open we us for in Flexion’s our call. all our you on update call second an will performance thank ZILRETTA’s Today, discuss up quarter, Q&A. earnings and we Scott, launch, then Thanks, activities, the clinical QX review
increase by to as sales earnings progress over press we in ZILRETTA’s sales million, a approximately strong QX. As see $X.X reflected of the XX% represents with second which in release, we in launch our continue quarter, net reported
provides ZILRETTA with is half made we track. work progress ZILRETTA’s the on we’ve physicians. introduction the we of it the hearing. team feedback building the share we their done very specific and bullish strong a our Q quarters in the remain In payer has commercial contacted strong seen based the on of clinical positive experiences launch advancing first they And foundation ZILRETTA. have early is continue And with pleased awareness code still to-date, ZILRETTA’s to a that directly days for about we’re who second XXXX. about patients While remain coverage with be The of to want physicians by and vein positive clinical stories the and potential second
since many anecdotal who us of ZILRETTA’s our are confidence a and moving potential in millions is predominantly confront buy the these year of deepens make OA XXXX reimbursement, painful of we physicians type product. patients respect With that profoundly knee. for While meaningful of the this as feedback be and have a a will for inspires and need to reimbursed difference foundational to conviction obviously they gain described further to ZILRETTA, which bill
On see continue service. our through forward to commercial coverage the flex we front, strong payer
of the code half we reported have that critical will ZILRETTA we a driver approximately reimbursement introduction such anticipate ZILRETTA’s the which As as receiving be we January. previously for J market, specific represents Medicare as And product J believe code. of most next
relatively that Q market more codes the majority research commercial code makes Q payers Q our X. Furthermore, on to code also decision However, the specific since was indicates a effective a consistent. CMS development, said welcome July code. reimbursement own simpler, uncommon. made for Q are as our issue on the became call utilize faster ZILRETTA expected are vast of ZILRETTA, we This earnings which discussed very last and to specific product That
with is prescribers fundamental personnel. of So level required that’s education their a there and office
will staff in the included to office code. large to their want institutions payment orthopedic practices on Similarly, work get Additionally to confirmation physicians with the formularies. of see we their Q ZILRETTA continue utilizing and
We internal processes. accounts interactions months. many making multiple these area require are good But progress their span intricacies navigate of in that can of to and this continue the
focus So this for our remains teams. an area of
usual, launch in As much more our detail. Dan will discuss activities
peak This we Why profiles of systemic appropriate both of ten-fold point, an adverse immediate the as the exposure indicating knees Phase in Furthermore knee view concerns place? OA triamcinolone release at pharmacologic ZILRETTA did the in for both on that the first in like I we excessive data the high treated reduced in patients knees the data were compared Currently substantial bilateral systemic acetonide release and to a OA with of would knees of insight ZILRETTA this concurrent the pleased triamcinolone injections from patients from in for on So ZILRETTA generate exposure. treated lower immediate ZILRETTA that to our The in the patients pain steroid injections July approximately bilateral were the acetonide. with who and systemic triamcinolone a associated both would study show well both with triamcinolone for ZILRETTA injection release and immediate knee short completed concentrations and exposure. study acetonide concentrations with whether with provide press this visit In in avoid demonstrate groups. systemically. of am second I’d immediate generally visit in the plasma most on triamcinolone be our development safe and release level study injections ZILRETTA initial demonstrated X was with subsequent trial then injection one similar triamcinolone start trial event provide injections compared report receive our finding patients and performed other that to an bilateral based positive. that knee on evaluating the tolerated activities. of concurrent with to do clinical update would administration results To into steroid pharmacokinetics of a bilateral to release today, clinical provided
these the interim which X-ray study soon as We for that data Phase was following weeks second results, at in XX. at repeat which evaluating between initial received tolerability XX show have as analysis that their and And time of the forward one average open-label of closed respect of baseline conference than of a weeks injection previously the patients and presented the in and dose compares ZILRETTA possible. radiographic data, medical We administration set of and more knee. XX overall presentation With later ongoing data a year. The recently year. second major this including to general full XB full dose results to after to XX% OA study the our we look submitted safety presenting
year. this to expect results We in make the fourth quarter available the of
open-label available results synovitis of fourth anticipate assessing currently year. the this has follow-up, open-label will and on SHIP enrolling Regarding as we of completed our Since progressed and IA OA PK with planned study, knee Xb, the a study of enrollment. shoulder in Phase of safety study patients as study patients the ZILRETTA The the quarter is OA ZILRETTA it the be injection weeks single in Phase in of with of X, administration we evaluating hip known or this the have the of of patients. XX has effect
in specific enrollment criteria eligibility the late results expect will take anticipated this and We time are consequently, XXXX. study for due various topline to
progress anticipate our of we is studies an receptor candidate, human toxicology inflammation product gene planned joint. we designed filing GLP Finally, within the is produce of to and FXXXX, antagonist, it successful, IND before and studies to are now first-in-human to we continue summary, clinical intra-articular advance initiating interleukin-X pleased turn are therapy clinical with preclinical our whenever the both trials and present which in If an over on-track Dan. share XXXX. on to the In SHIP year-end. trials we updates administration studies I’ll the repeat are