OliX Pharmaceuticals Announces Positive Results from a Phase 2a Trial of OLX10010 for Hypertrophic Scar Treatment
OliX Pharmaceuticals, a leading developer of RNAi therapeutics, today announced positive headline results of a phase 2a trial study in the treatment of hypertrophic scars which met the primary observer-based endpoint at week 24 as evaluated by the Patient and Observer Scar Assessment Scale (POSAS). The trial ascertained the effects of intradermal OLX10010, initiated 2 weeks after surgery and administered biweekly over 12 weeks versus placebo in adult patients with hypertrophic scars. This trial uses a randomized, double-blind, placebo-controlled, multi-center, intrasubject trial design and continues until week 48 after surgery.
The data shows that 24 weeks after scar excision surgery relative to baseline, the biweekly intradermal administration of OLX10010, but not placebo, leads to significant improvement of hypertrophic scar appearance (see Figure 1 + 2) on both, the POSAS observer global score (p=.0017, 2-sided) and the POSAS observer total score (p=.029, 2-sided). There was no clear evidence for dose-dependent (2mg and 5mg) effects. Follow-up of participating patients up to 48 weeks post-surgery is ongoing.
The trial confirms the safety and tolerability of OLX10010 at both dose levels, with no safety issues identified. Also, no negative effects on wound-healing after surgery were observed. The absence of any safety concerns stimulates development of OLX10010 as monotherapy or in combination with other treatments for hypertrophic scars, a condition for which currently available treatments are deemed insufficient.
Dr Waibel, University of Miami Miller School of Medicine and Subsection Chief of Dermatology, Baptist Hospital of Miami, and Miami Dermatology & Laser Institute, who participated in this trial stated: “The treatment of hypertrophic scars remains elusive to date with no targeted treatments available for this large patient population. Connective tissue growth factor (CTGF) plays an important role in fibrosis. CTGF inhibitors, like OLX10010, have inherent advantages with providing an evidence-based treatment approach and practical advantages of allowing new mechanisms of action and less frequent administration. The safety data observed in this trial are particularly encouraging positioning OLX10010 as potential first-in-line treatment for this indication.”
Dong Ki Lee, Ph.D., Founder and Chief Executive Officer of OliX Pharmaceuticals, said: “Hypertrophic scarring is a significant concern for patients and a challenging problem for clinicians. With at present no treatment modalities allowing sufficient treatment of hypertrophic scars, this condition presents a major unmet medical need with a significant compound annual growth rate. We are excited about the initial results from this trial, supporting the development of OLX10010 as backbone treatment for patients with hypertrophic scars, when used alone and in combination with standard of care and future novel treatments.”
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