Lead program
Amyotrophic lateral sclerosis (ALS)
Lead indication. SRSF3-directed antisense designed to release translational repression of selected innate immune transcripts in microglia/macrophages.
Pipeline
RNOVA Tx is advancing an SRSF3 platform led by ALS, supported by a next-generation cell-targeted delivery strategy. All programs are at the research and preclinical stage.
Lead indication. SRSF3-directed antisense designed to release translational repression of selected innate immune transcripts in microglia/macrophages.
Exploring the relevance of the SRSF3 checkpoint in neurodegenerative conditions beyond ALS.
Cell-selective delivery strategy under development, designed to improve access of SRSF3-directed antisense to selected innate immune cells.
Development stages are shown only once confirmed. A dashed track means the stage has not yet been published.
Pipeline
Amyotrophic lateral sclerosis (ALS)
Lead indication. SRSF3-directed antisense designed to release translational repression of selected innate immune transcripts in microglia/macrophages.
Related neurodegenerative diseases
Exploring the relevance of the SRSF3 checkpoint in neurodegenerative conditions beyond ALS.
Multiple CNS opportunities
Cell-selective delivery strategy under development, designed to improve access of SRSF3-directed antisense to selected innate immune cells.
No RNOVA Tx program has entered clinical trials. Program names, indications and stages will be updated as they are confirmed.
04 Targeted RNA therapeutics
Antisense strategy
SRSF3-directed antisense oligonucleotides conjugated to a cell-penetrating peptide to support uptake into immune cells. Built on the target biology described in RNOVA’s published research and foundational patent.
Next-generation targeting
An emerging cell-targeted delivery strategy designed to improve therapeutic access of SRSF3-directed antisense to selected innate immune cell populations.
RNOVA Tx welcomes conversations with pharmaceutical, biotechnology, scientific and development partners interested in RNA therapeutics and neurodegenerative disease.