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NSAIDs are increasingly employed in acute pain management to replace opioids, and as a component of multimodal analgesia, a growing practice whereby multiple drugs are administered to achieve optimal pain reduction in post-operative settings. While today’s NSAIDs are effective, they can cause a range of GI-related adverse effects. Even in short-term use, they triple the risk of serious GI outcomes.2 Celecoxib (branded as Celebrex) offers some improvement in GI safety, but its use is associated with cardiovascular toxicity. Beyond considerations of addiction and abuse, opioids can cause adverse GI effects, including nausea, vomiting and severe constipation—leading to patient discomfort and the cost of extended hospitalization.3
The drug remained GI-safe when administered to animals with compromised mucosal defense or pre-existing ulcers—situations in which today’s NSAIDs (including celecoxib) can cause ulcers and bleeding in humans. Otenaproxesul also remained safe when co-administered with aspirin. In addition, otenaproxesul did not elevate blood pressure when administered to rats with hypertension, in contrast to naproxen’s hypertensive effect.
In 2018, Antibe completed a Phase IIB GI safety trial of otenaproxesul in 244 healthy volunteers. It was designed to demonstrate superiority of otenaproxesul compared to naproxen, one of the most prescribed NSAIDs. One group was treated for 14 days with otenaproxesul (250 mg, once daily), while the other group was treated for the same period with the standard prescription dose of naproxen (550 mg, twice daily, totaling 1,100 mg per day). The study’s primary endpoint was the incidence of gastric or duodenal ulcers of at least 3 mm diameter with unequivocal depth, considered the ‘gold standard’ in assessing the GI safety of NSAIDs.
Otenaproxesul successfully met the primary endpoint in the study. Subjects on otenaproxesul exhibited an ulceration rate of 2.5% (3/118) versus an ulceration rate of 42.1% (53/126) for subjects on naproxen at the end of the treatment period, with a very high degree of statistical significance (p<0.0001).
In June 2020, Antibe reported positive top-line results from its Phase IIB dose ranging, efficacy study designed to validate the efficacy of otenaproxesul in reducing chronic pain. The study involved 384 participants across 39 sites.
Subjects were randomized to placebo or one of three doses of otenaproxesul administered once daily: 150 mg, 200 mg or 250 mg. The primary endpoint was the change in the WOMAC pain subscale scores (the ‘gold standard’ in chronic pain assessment) over a 14-day treatment period. The results showed a high degree of statistical significance for the 200 mg and 250 mg doses, thereby demonstrating efficacy in pain reduction. The lowest dose, although not powered for statistical significance, showed a positive trend toward efficacy.
Further validating the WOMAC pain measures, otenaproxesul delivered profound COX inhibition, exceeding 90% for all doses, at very high degrees of statistical significance (p<0.0002).
The chart above depicts the pain efficacy of otenaproxesul in a 14-day treatment regimen for three doses. The vertical bars depict the improvement in WOMAC pain subscale scores for each of the doses after two weeks of administration. The horizontal dotted line indicates the average efficacy of NSAIDs after 12 (or more) weeks, as set out in Comparative Pain Reduction of Oral Non-steroidal Anti-inflammatory Drugs and Opioids for Knee Osteoarthritis: Systematic Analytic Review; Osteoarthritis and Cartilage, S.R. Smith et al., 2016.5
These results support the success of an earlier Phase IIA open-label, effectiveness study. Its primary endpoint was the clinical assessment of pain over the ten-day course of treatment at 250 mg once-daily (n = 12), delivering a significant WOMAC pain score reduction on day 10, at a very high level of statistical significance in comparison to baseline pain (p<0.001).
Using post-operative pain as a regulatory pathway, Antibe is leveraging otenaproxesul’s extensive GI safety and efficacy data to de-risk and accelerate the drug’s development.
Since launching the clinical program for acute pain in early 2022, Antibe has transitioned to a faster-dissolving formulation. The new formulation’s benefits include: (i) rapid dissolution mechanics, accelerating otenaproxesul’s onset of action, a key benchmark for acute pain medications; and (ii) enhanced bioavailability, enabling a significant dose reduction compared to its previous formulation and a potential pathway to address chronic pain indications.
Antibe plans to conduct a single Phase II trial utilizing a surgical bunionectomy model, recognized as one of the most reliable methods for evaluating analgesic efficacy in post-operative pain.
Upon success of the Phase II trial, Antibe will request an End of Phase 2
Post-operative pain serves as an ideal regulatory pathway to the broader acute pain market. With the lack of recent innovation in oral analgesics and the urgent need for non-addictive alternatives, Antibe expects otenaproxesul to be especially attractive to potential partners.
Further information about otenaproxesul’s commercial opportunity is available in our Corporate Presentation.
meeting with the US FDA to discuss the Phase III program. Given the short treatment durations in acute pain trials, we anticipate that the Phase III program can be completed within 15 months of initiation. This includes two concurrent, pivotal efficacy trials to assess post-operative pain relief for the following surgical procedures: (i) the hard-tissue model of bunionectomy, replicating the Phase II trial with a larger sample size; and (ii) abdominoplasty, a widely accepted soft-tissue surgical model. Following Phase III, Antibe intends to apply for marketing approval for a broad acute pain indication.
Antibe is also investigating alternative dosing regimens as a potential path forward for chronic indications.
1. Allied Market Research, Biotech Advisors, DataBridge, DelveInsight, GlobalData, Statista, Transparency Market Research, Antibe internal estimates.
2. Fine M, Am J ManagCare (2013);19(16 suppl):S267-S272.
3. Whitman CJ et al., J Opioid Manag (Sep-Oct 2015)11(5):383-91.
4. Post hoc analysis. Results do not necessarily predict future efficacy results.
5. Smith SR et al., Osteoarthritis and Cartilage (2016);24: 962-972.