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www.nephjc.com/news/...
I want more info: Check out #NephJC summary by @notjustdialysis.bsky.social
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A figure paints🖼️ a 1000 words!
Emerging evidence from APRIL/BAFF–axis trials underscores how central this pathway is to IgAN biology. Let’s put ORIGIN side by side with the others and see what we learn!
We recently got to hear the patient voice from @jonathanpollack.bsk.social
About his journey with IgAN and his excitement for a future of precision medicine while also calling for greater worldwide equity.
We recently got to hear the patient voice from @jonathanpollack.bsk.social
About his journey with IgAN and his excitement for a future of precision medicine while also calling for greater worldwide equity.
Although this is an exciting time with the FDA approving new therapies for IgAN rapidly - they are mostly not available or accessible outside a few select countries -especially in places like Asia where the bulk of IgAN patients live.
Implementation and equity have entered the chat.
Although this is an exciting time with the FDA approving new therapies for IgAN rapidly - they are mostly not available or accessible outside a few select countries -especially in places like Asia where the bulk of IgAN patients live.
Implementation and equity have entered the chat.
Overall, these interim results suggest that APRIL-based and BAFF/APRIL–based therapies may represent important future disease-modifying options in IgAN
A full throated, “Hallelujah” being reserved until eGFR data is finalized.
Overall, these interim results suggest that APRIL-based and BAFF/APRIL–based therapies may represent important future disease-modifying options in IgAN
A full throated, “Hallelujah” being reserved until eGFR data is finalized.
Whether dual inhibition APRIL/BAFF offers a longer-term advantage over APRIL-selective therapy remains a key question that only eGFR slope data will answer. APRIL-selective therapy also prevents its action at other receptors (BCMA).
Do you think either has the advantage?
Whether dual inhibition APRIL/BAFF offers a longer-term advantage over APRIL-selective therapy remains a key question that only eGFR slope data will answer. APRIL-selective therapy also prevents its action at other receptors (BCMA).
Do you think either has the advantage?
As newer trials such as APPLAUSE-IgAN (iptacopan) & NEFIGARD (budesonide) continue to illuminate parts of the cascade, the APRIL–BAFF pathway stands out as the most direct attempt to target the source of pathogenic IgA production.
Will this class of meds become foundational in IgAN?
As newer trials such as APPLAUSE-IgAN (iptacopan) & NEFIGARD (budesonide) continue to illuminate parts of the cascade, the APRIL–BAFF pathway stands out as the most direct attempt to target the source of pathogenic IgA production.
Will this class of meds become foundational in IgAN?
from the high impact trial session - this was a great study design
The India ALLIANCE GRACE IgAN trial
Lead by Succeena Alexander from CMC Vellore
#NephSky
1/
In VISIONARY, APRIL-selective B-cell inhibition ⬇️proteinuria & IgA-related biomarkers, confirming APRIL’s key pathogenic role.
In ORIGIN-3, atacicept’s BAFF + APRIL blockade targets earlier B-cell checkpoints, dismantling both the production & maintenance of aberrant IgA response.
In VISIONARY, APRIL-selective B-cell inhibition ⬇️proteinuria & IgA-related biomarkers, confirming APRIL’s key pathogenic role.
In ORIGIN-3, atacicept’s BAFF + APRIL blockade targets earlier B-cell checkpoints, dismantling both the production & maintenance of aberrant IgA response.
The emerging evidence from APRIL/BAFF–axis trials (including VISIONARY (sibeprenlimab) & ORIGIN-3 (atacicept)) highlight how central this pathway is to the mechanisms of IgAN.
The emerging evidence from APRIL/BAFF–axis trials (including VISIONARY (sibeprenlimab) & ORIGIN-3 (atacicept)) highlight how central this pathway is to the mechanisms of IgAN.
This interim analysis produced clear improvements in key biomarkers of IgAN.
The magnitude of the proteinuria reduction & parallel drop in Gd-IgA1 support the idea that atacicept is acting directly on the drivers of disease, rather than through non-specific hemodynamic effects.
This interim analysis produced clear improvements in key biomarkers of IgAN.
The magnitude of the proteinuria reduction & parallel drop in Gd-IgA1 support the idea that atacicept is acting directly on the drivers of disease, rather than through non-specific hemodynamic effects.
It’s not PLA2R or ANCA even as a biomarker
#NephJC
See bsky.app/profile/hswa...
But the Gd-IgA doesn’t seem so impressive to me?
journals.lww.com/cjasn/pages/...
#NephSky @asnpublications.bsky.social #CJASN
VA by @corinateodosiu.bsky.social
It’s not PLA2R or ANCA even as a biomarker
#NephJC
See bsky.app/profile/hswa...
2° Endpoints
📉Atacicept reduced Gd-IgA1 by 68.3% at week 36 vs 2.9% with placebo, as early as week 4
🩸Among patients with baseline ≥1+ hematuria, 81% in the atacicept group achieved resolution vs 21% with placebo arm
🥤UACR ratio fell by 47.3% in atacicept vs 8.8% with placebo
2° Endpoints
📉Atacicept reduced Gd-IgA1 by 68.3% at week 36 vs 2.9% with placebo, as early as week 4
🩸Among patients with baseline ≥1+ hematuria, 81% in the atacicept group achieved resolution vs 21% with placebo arm
🥤UACR ratio fell by 47.3% in atacicept vs 8.8% with placebo
📉The decline in proteinuria was already evident by week 12 & continued thru week 36
🚨Prespecified subgroup analyses showed that this benefit was consistent across all categories, including age, sex, region, race, baseline UPCR/ eGFR & SGLT2i use
📉The decline in proteinuria was already evident by week 12 & continued thru week 36
🚨Prespecified subgroup analyses showed that this benefit was consistent across all categories, including age, sex, region, race, baseline UPCR/ eGFR & SGLT2i use
1° Endpoint
At week 36- 🗓️
📉Atacicept: 24-hour urinary protein-to-creatinine ratio decreased by 45.7%
🔻Placebo: 24-hour urinary protein-to-creatinine ratio decreased by 6.8%
1° Endpoint
At week 36- 🗓️
📉Atacicept: 24-hour urinary protein-to-creatinine ratio decreased by 45.7%
🔻Placebo: 24-hour urinary protein-to-creatinine ratio decreased by 6.8%
99.5% of patients were already receiving the max tolerated dose of a RASi at baseline, & just over half (53.2%) were #flozinated
About 60% had 1+ or more hematuria, with proteinuria 2 g/day & preserved GFR (60 ml/min).
Are these the patients you most often encounter with IgAN?
99.5% of patients were already receiving the max tolerated dose of a RASi at baseline, & just over half (53.2%) were #flozinated
About 60% had 1+ or more hematuria, with proteinuria 2 g/day & preserved GFR (60 ml/min).
Are these the patients you most often encounter with IgAN?
A total of 203 participants were included in the 36-week interim efficacy analysis, with 106 patients receiving atacicept and 97 patients receiving placebo.
A total of 203 participants were included in the 36-week interim efficacy analysis, with 106 patients receiving atacicept and 97 patients receiving placebo.