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ARA 290

Cibinetide, PHBSP, PH-BSP, Helix B surface peptide

Quick Stats
Studies 51
Trials 5
Score 3
2017 pubmed 90 citations

Cibinetide Improves Corneal Nerve Fiber Abundance in Patients With Sarcoidosis-Associated Small Nerve Fiber Loss and Neuropathic Pain.

Culver. Daniel A DA; Dahan. Albert A; Bajorunas. Daiva D; Jeziorska. Maria M; van Velzen. Monique M; Aarts. Leon P H J LPHJ; Tavee. Jinny J; Tannemaat. Martijn R MR; Dunne. Ann N AN; Kirk. Rita I RI; Petropoulos. Ioannis N IN; Cerami. Anthony A; Malik. Rayaz A RA; Brines. Michael M

Key Findings

  • Cibinetide 4 mg/day increased corneal nerve fiber area by about 700 µm², a statistically significant change.
  • Skin nerve regeneration (GAP‑43+ fibers) rose significantly only in the 4 mg group.
  • Improvements in nerve fiber measures correlated with better 6‑minute walk test performance and reduced neuropathic pain.

Practical Outcomes

  • For biohackers interested in nerve health, the study suggests a 4 mg daily dose of cibinetide for about a month may promote small‑fiber regeneration and relieve neuropathic pain, at least in a sarcoidosis context. However, the drug is not yet widely available and the results are specific to a disease population, so broader use in healthy individuals remains unproven.

Summary

A 28‑day trial in people with sarcoidosis‑related nerve loss showed that taking the drug cibinetide (also called ara‑290) at 4 mg a day can grow tiny nerve fibers in the eye and skin, and this growth was linked to better walking ability and less pain. The effect was strongest at the 4 mg dose, while lower or higher doses were less clear.

Abstract

Sarcoidosis frequently is complicated by small nerve fiber loss (SNFL), which can be quantified using corneal confocal microscopy (CCM). Prior studies suggest that the innate repair receptor agonist cibinetide reverses corneal nerve loss. This phase 2b, 28-day, randomized trial of 64 subjects with sarcoid-associated SNFL and neuropathic pain assessed the effect of cibinetide on corneal nerve fiber area (CNFA) and regenerating intraepidermal fibers (GAP-43+) as surrogate endpoints for disease modification, pain severity, and functional capacity (6-minute walk test [6MWT]). Cibinetide (1, 4, or 8 mg/day) was compared to placebo. The primary study endpoint was a change in CNFA at 28 days. The placebo-corrected mean change from baseline CNFA (μm2) at day 28 was 109 (95% confidence interval [CI], -429, 647), 697 (159, 1236; P = 0.012), and 431 (-130, 992) in the 1, 4, and 8 mg groups, respectively. Intraepidermal GAP-43+ fibers increased in the 4 mg group (P = 0.035). Further, changes in CNFA correlated with changes in GAP-43+ (ρ = 0.575; P = 0.025) and 6MWT (ρ = 0.645; P = 0.009). Pain improved significantly in all groups, with subjects having moderate-severe pain reporting a clinically meaningful placebo-corrected decrease in pain intensity in the 4 mg group (P = 0.157). Cibinetide significantly increased small nerve fiber abundance in the cornea and skin, consistent with a disease modifying effect. The relationships between CNFA and other clinical measures of disease support its use as a surrogate endpoint to assess potential disease modifying therapies for neuropathy.

Study Information

Provider

pubmed

Year

2017

Date

2017-05-01T00:00:00.000Z

DOI

10.1167/iovs.16-21291

Citations

90

References

47