you, everyone, for And joining us. Ryan. you, thank Thank
program with marked and continued the expectations. in line in by launch been quarter second development progress, of in HEPLISAV-B up our and immuno-oncology under has The both our
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customer to illustrate involved. examples of us Now case many to individual investors frames studies the provide asked have time
XXX threefold meetings quarter pathway. targeted has XX decisions customer important ordered the helpful the the and implemented think the XX At customers or how one. larger of processes fully we understand second, is sales customers of strength complex the an now HEPLISAV-B purchase over quarter one $X.X but future and is ordered quarter system. are a and the we have examples visits yes, been whom, P&T use HEPLISAV-B customers quarter and and two hopefully, that resulted that sevenfold of some increase becoming make the have end had one; their powerful things: I will field run XXX, seeing indicated strong label all beyond their the Currently, have that decision-making. today, also beyond in X one, processes, the among I've review, how provide, the myself, understanding, At diary, in so over subcommittee HEPLISAV-B most two of the that most and a us digressed that we of throughout frustrating; that the I promising million our position, along lead in can call, whom, had conducting over quarter HEPLISAV-B, quarter -- our think That of be ultimately, do eightfold customer continued accounts, Firstly, very XX to first I influencer increase HEPLISAV-B had one; we today, addition, now had implemented is XX P&T system. reported and XX increase they customers throughout the In of number vaccine movement these P&T quarter of
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oncology to move our busy a on oncology. me has period Quarter two also for programs. Let
We TLRX combination our are anti-PD-X with currently trials running X therapies. with agonists in
trial with Our Phase and both with SD-XXX advanced trial and naïve neck, a and therapy. and II advanced melanoma pembrolizumab combining experienced is head includes anti-PD-X SYNERGY patients to
cancer. I enrolling DVXXX, with in inhaled study Phase safety with Additionally, cell also our therapy combining agonist, an anti-PD-X we lung patients are non-small TLRX
those at updates head advanced SYNERGY, and anti-PD-X. therapy showing expected overall naïve rate meetings data And an At with in significant with toxicities provided from to cancer. we the neck well tolerated rates, higher data we had head and We of than key in in two, monotherapy observed. dose-limiting combination melanoma best quarter encouraging patients XX%. During AACR response neck no April, and both pembrolizumab presented response was
or X overall, an KEYTRUDA, Phase of melanoma months outperformed X These June. Additionally, to focused we rate patients data this XX%. comparison response In X naïve an with in and the provided advanced anti-PD-X update XX X combination X in with on of our survival X clearly SD-XXX II doses XX% milligrams milligrams in SD-XXX. milligrams of data of progression-free of of at ASCO milligram analysis,
SYNERGY Importantly, patients both include we the at neck in melanoma We've who head PD-LX -- all PD-X baseline previously anti-PD-X and received of of the patients arms positive -- and also a XX. X-milligram X in study, negative expanded to out was therapy. this regimen the noted response that have including of enrollment positive
progress. Looking we updates the opportunity will half the the provide forward our second to of to have year, on
We to October. accepted that have at report X ESMO abstracts been are in pleased
reached for patients includes We X-milligram, have at not more II at have all completed second initial all naïve which about enrollment may that to the the therapy, point. present recognizing XX but targeted that of patients the will Phase and scan XX anti-PD-X data melanoma
in naïve Additionally, and neck both experience and will with patients data anti-PD-X of head anti-PD-X melanoma interim prior therapy. present we to
set encouraging data into of to This design the selection Merck, clinical for Phase with early the discuss will to plan and forward clinical of III With options, partnership and FDA the progression trial. III. tumor under meeting a expansion types expanding melanoma we study [Technical neck, us additional partner, this allow with assessing of these look promising generated results and best data Phase head the and by Difficulty] SD-XXX to and options of our in meet summer to results
for these our to forward by be and expect identify end mature. We able year path discussions results once you to specific
quarter results. Ostrach, describe Our two our now will CFO, Michael financial