Biopharma’s continuous efforts to conquer immunoglobulin A nephropathy (IgAN), also called Berger's disease, were on full display at the American Society of Nephrology's Kidney Week 2022 this weekend.
Roche and Ionis Head to Phase III
Following positive Phase II data, Roche is planning to take an Ionis-developed antisense drug candidate into a late-stage clinical trial in the first part of 2023.
Ionis presented positive data Sunday from a Phase II trial assessing IONIS-FB-L as a potential treatment for patients with immunoglobulin A nephropathy (IgAN), also known as Berger’s disease. Data showed the drug candidate reduced proteinuria by 44% after 29 weeks. In addition, Ionis reported:
- Kidney function as measured by estimated glomerular filtration rate was maintained.
- The drug led to “robust and sustained reductions” in plasma complement Factor B, alternative pathway activity (AH50) and urinary complement fragment Ba (Factor Ba).
- A favorable safety and tolerability profile was maintained.
IONIS-FB-L uses Ionis’ LIgand Conjugated Antisense (LICA) technology. It is designed to reduce the production of complement factor B, a key protein in the complement innate immune system. Over-action of the FB protein is associated with the development of multiple complement-mediated diseases, including IgAN.
Roche and Ionis teamed up in July on the development of IONIS-FB-L in IgAN.
Chinook’s IgAN Treatment Also Moves Forward
Seattle-based Chinook Therapeutics shared data from its ongoing Phase I/II trial evaluating BION-1301, a novel anti-APRIL monoclonal antibody.
Blocking APRIL is a potentially disease-modifying approach to treating IgAN, as it reduces circulating levels of galactose-deficient IgA1 (Gd-IgA1), Chinook stated in the press release.
Data from two cohorts treated in the study showed BION-1301 generated “rapid and sustained” reductions in IgA and Gd-IgA1 levels, the company announced Friday.
- In cohort 1: intravenous treatment with BION-1301 showed significant reduction of proteinuria throughout the study. At 12 weeks, proteinuria was reduced by 30.4%. At 24 weeks, the reduction increased to 48.8%. By 52 weeks, reduction had reached 66.9%.
- In Cohort 2, patients received a subcutaneous version of BION-1301. Data showed mean proteinuria reductions of 28.7% in 15 patients at 12 weeks of treatment. Reduction levels increased the longer patients remained on treatment. At 24 weeks, nine patients showed a 53.8% reduction.
Eric Bebmeiher, president and chief executive officer of Chinook, said the reductions observed to date are highly consistent between both cohorts. Based on this data, Bebmeiher said the company intends to move forward with a Phase III trial in IgAN next year.
Vera’s Atacicept Reduces Immune Complex Levels
On Saturday, Brisbane, Calif.-based Vera Therapeutics shared data from its Phase IIa JANUS study that showed atacicept reduced immune complex levels in patients with IgAN.
Vera claimed atacicept is the first therapeutic to show a reduction in the first three hits of IgAN pathogenesis: serum galactose-deficient IgA1 (Gd-IgA1), anti-Gd-IgA1 and immune complex levels.
In its presentation, Vera noted that Gd-IgA1 plays a central role in IgAN pathogenesis. Antibodies that develop in the hinge region of Gd-IgA1 lead to formation of immune complexes that deposit in the kidney and cause progressive renal injury. Data from the JANUS study showed atacicept decreased circulatory Gd-IgA1 in IgAN patients and led to a reduction of anti-Gd-IgA1 antibodies.
IgAN has become a highly contested area for multiple companies. An estimated 400,000 people suffer from IgAN across the United States and Europe. About half of these patients are expected to develop end-stage renal disease within 20 years from initial diagnosis, which will lead to dialysis or kidney transplant.
Last year, Calliditas Therapeutics’ Tarpeyo became the first approved medication to decrease urine protein in IgA nephropathy.
https://www.biospace.com/article/roche-ionis-chinook-and-vera-move-forward-in-igan-/
No comments:
Post a Comment
Note: Only a member of this blog may post a comment.