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Sovateltide for the Treatment of Acute Traumatic Brain Injury (RESTORE-TBI)

2026年10月7日 更新者:Pharmazz, Inc.

A Prospective, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase III Clinical Study to Assess the Efficacy and Safety of Sovateltide in Patients With Traumatic Brain Injury

Traumatic brain injury (TBI) remains a leading cause of global disability, yet current clinical management is limited to supportive care and pressure stabilization using hyperosmolar therapies like mannitol and hypertonic saline. These strategies fail to address the destructive cellular cascades that persist long after the initial impact, leaving 66.3% of severe TBI patients with permanent cognitive and neurological deficits. To bridge this critical unmet medical need, the therapeutic focus must shift toward neuroprotective and neuroregenerative agents that actively block secondary injury cascades such as excitotoxicity, apoptosis, and chronic neuroinflammation.

Sovateltide is a selective endothelin-B receptor agonist. It was previously reported to reduce apoptosis, stimulate neurogenesis, and improve functional recovery. Unlike most TBI candidates restricted to preclinical phases, sovateltide possesses a robust human safety and tolerability profile established across Phase I, II, III, and IV ischemic stroke trials.

We conducted a preclinical study in Wistar rats with induced TBI and showed that sovateltide effectively preserved BBB integrity, a critical determinant of post-injury outcomes, and significantly reduced neuronal apoptosis, as evidenced by decreased expression of caspase-3 and caspase-6, key markers of programmed cell death. Treated animals also exhibited notable improvements in neurobehavioral performance, reflecting functional recovery likely attributable to the drug's antioxidant, anti-inflammatory, and anti-apoptotic mechanisms. These results align with earlier evidence showing that ETB receptor activation enhances angiogenesis, neurogenesis, and synaptic remodeling, processes essential for neural repair following brain injury.

The present study has been designed to advance sovateltide (IRL-1620) into a pivotal Phase III clinical trial for acute traumatic brain injury (TBI). With millions affected annually and zero approved neuroprotective pharmacotherapies available, this milestone marks a critical step forward in addressing one of modern medicine's greatest unmet needs. By harnessing our proprietary neural repair discovery platform, sovateltide targets the cascade of secondary cell death while stimulating neurogenesis and angiogenesis. Building on the strong momentum of our ongoing global Phase III RESPECT-ETB study in acute ischemic stroke, this study will further validate the broad therapeutic potential of our endothelin-B receptor platform across severe acute neurovascular conditions.

研究概览

地位

尚未招聘

详细说明

A traumatic brain injury (TBI) is a form of brain damage that results from an external mechanical force impacting the head or body, such as a sudden blow, jolt, or wound. The injuries could be penetrating (open) ones - commonly seen in motor vehicle accidents, falls, sports injuries, and explosive blasts in which an object such as a bullet, shrapnel, or bone fragment breaches the skull and directly damages brain tissue, or non-penetrating (closed or blunt) ones, which result from rapid acceleration, deceleration, or rotational forces that cause the brain to move within the skull. Based on the timing of the impact and damage, these injuries are categorized as primary or secondary. Primary injuries, such as contusions, lacerations, or hemorrhage, occur at the moment of impact and involve immediate damage. Secondary injury develops over time through complex biochemical and physiological processes such as increased intracranial pressure, cerebral edema, ischemia, excitotoxicity, oxidative stress, and neuroinflammation, which can worsen neurological outcomes later.

According to the Global Burden of Diseases database in 2021, there were 20.84 million incident cases and 37.93 million prevalent cases of TBI worldwide. Between 1990 and 2021, the global number of TBI incidents and prevalent cases increased by 22.6% and 53.3%, respectively; however, the age-standardized incidence rate declined by 0.11%. These rates generally increased with age and were higher in males than in females. The highest age-standardized prevalence and years lived with disability rates were observed in Eastern and Central Europe. Globally, falls were the leading cause of TBI in 2021, followed by road injuries, violence, and exposure to mechanical forces.

Currently, no therapeutic agent is approved for TBI because of the injury's biological complexity, heterogeneity in patient presentation, and limited translation of preclinical success into human trials. Hence, future progress likely depends on developing drugs or combination therapies with multimodal mechanisms of action that support neural cell protection, regeneration, repair, and functional restoration. Moreover, TBI pathophysiology is complex, involving vascular damage, inflammation, apoptosis, and other processes that trigger neuronal damage and death. A thorough understanding of TBI pathophysiology is essential for developing novel therapeutic agents that provide neuroprotection by curbing inflammation, enhancing angiogenesis, reducing hypoxic episodes, excitotoxicity, and apoptosis, and promoting neuroregeneration in injured brain tissue. Endothelin signaling regulates these pathophysiological events in the mammalian neurovascular system; therefore, the endothelin system could be a potent drug-development target in TBI.

Sovateltide (TycamzziTM, IRL-1620, PMZ-1620) is a first-in-class ETB receptor agonist approved in India for treating acute ischemic stroke (AIS), promoting neuroprotection and regeneration via neuron and blood vessel growth. We evaluated the neuroprotective potential of sovateltide in the Marmarou weight-drop rat model of traumatic brain injury (TBI). TBI onset in rats damaged blood-brain barrier (BBB) and increased brain water content, inflammation and oxidative stress. Neuronal damage in the prefrontal cortex and hippocampal subfields (CA1-CA3 and dentate gyrus) was seen on day 1 post-injury. A marked increase in Neurobehavioral Severity Score-Revised (NSS-R), indicating neurological impairment, was also observed. Rats were either treated with sovateltide (5μg/kg) or mannitol (20% w/v) or Normal Saline (5ml/kg) administered three times a day on 1st, 3rd and 6th day after induction of TBI. Animals treated with sovateltide or mannitol showed progressive functional recovery with a significantly reduced NSS-R score compared to untreated TBI rats by day 7. These animals also showed a clear trend toward behavioral improvement; however, anxiety levels and locomotor activity remained comparable. Damage to the BBB, reflected by elevated Evans Blue Dye elution, was substantially reduced in sovateltide-treated rats. Sovateltide exhibited antioxidant activities and reduced malondialdehyde (MDA) levels, restoring superoxide dismutase (SOD), catalase (CAT), and glutathione (GSH) levels to near-normal. Sovateltide-treated rats had decreased inflammatory indicators/mediators (e.g., NF-κB, IL-6, and TNF-α) compared with untreated and mannitol-treated animals. At the tissue level, sovateltide-treated animals had better-preserved neural tissue architecture, like sham animals, than control and mannitol-treated animals. Apoptotic markers caspase-3 and caspase-6 were significantly reduced in sovateltide animals, along with attenuation of astrocytic activation indicated by decreased GFAP in cortical and hippocampal regions. Thus, sovateltide confers multimodal neuroprotection by alleviating oxidative stress, suppressing neuroinflammation, preserving BBB integrity and neuronal morphology, and inhibiting apoptosis following TBI.

A TBI study in Wistar rats found that sovateltide preserved BBB integrity and reduced apoptosis, as evidenced by decreased caspase-3 and caspase-6 expression and improved neurobehavioral outcomes, likely due to its antioxidant and anti-apoptotic properties. Overall, studies show that the endothelin system, particularly ETB receptor signaling, represents a promising therapeutic axis that can address TBI heterogeneity by integrating vascular protection, anti-inflammatory effects, and neural regeneration. Unlike traditional monotherapies that target isolated pathways, ETB activation through sovateltide would offer a multimodal approach to target the full spectrum of TBI, from acute neuroprotection to long-term neural repair.

  • Sovateltide stimulates ETB receptors, which are highly expressed during neural development. Research indicates that activating these receptors in the adult brain enhances NPC proliferation and differentiation into mature, functional neurons.
  • Effective neurogenesis requires a robust blood supply. Sovateltide promotes the formation of new micro-vessels (angiogenesis) by increasing levels of Vascular Endothelial Growth Factor (VEGF) and Nerve Growth Factor (NGF). This ensures that the "new" brain tissue has the oxygen and nutrient support needed to survive and integrate.
  • Sovateltide has been shown to inhibit the pathways that lead to delayed neuronal death. Protecting existing neurons in the "penumbra" (the area surrounding the core injury) limits the eventual size of the brain lesion.
  • Research suggests that Sovateltide enhances mitochondrial biogenesis and maintains mitochondrial membrane potential. Since TBI causes massive metabolic failure, stabilizing the cell's "powerhouse" is critical for preventing further tissue loss.
  • Stimulation of ETB receptors on the vascular endothelium triggers the release of nitric oxide, leading to vasodilation and improved perfusion to the injured regions.

The pathophysiological similarities between stroke and TBI-specifically the roles of ischemia, inflammation, and the need for remodeling-provide a strong "proof of concept" for the application of sovateltide in TBI.

研究类型

介入性

注册 (估计的)

214

阶段

  • 第三阶段

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 90年 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

A participant will be eligible for inclusion in the study if the participant fulfills the following criteria:

  1. Adult male or female aged 18-90 years
  2. Consent must be obtained prior to any study-specific procedure from the participant or, if the participant lacks capacity to provide informed consent, from the participant's Legally Authorized Representative (LAR), in accordance with applicable law and IRB requirements.
  3. Clinical diagnosis of closed traumatic brain injury (TBI), classified as moderate to severe, with a post-resuscitation Glasgow Coma Scale (GCS) score of 5 to 13, inclusive, at screening (moderate TBI: GCS 9-13; eligible severe TBI range: GCS 5-8).
  4. Radiological confirmation of TBI on neuroimaging (diffuse injury II-V, Marshall's CT Classification).
  5. At least one reactive pupil (pinpoint pupils due to opioid pain treatment are considered reactive).
  6. The participant is <48 hours from the time of TBI onset when the first dose of sovateltide is administered. The time of TBI onset is when the injury occurred.
  7. Reasonable expectation of availability to receive the full sovateltide course of therapy and to be available for subsequent follow-up visits.

Exclusion Criteria:

A participant will not be considered eligible for inclusion in this study if the participant meets any of the following exclusion criteria:

  1. TBI caused by penetrating injury (e.g., gunshot wound) rather than blunt trauma.
  2. Isolated epidural hematoma.
  3. Suspected or confirmed spinal cord injury.
  4. Severe cardiac or hemodynamic instability prior to randomization.
  5. Life expectancy of less than 72 hours as determined by the Investigator.
  6. Pregnant or lactating women.
  7. Known medical history of neurological (other than current TBI) or psychiatric condition that, in the investigator's opinion, would confound the neurological and functional evaluations, lead to further deterioration of neurological status, or interfere with participation in this study.
  8. Evidence of any other major life-threatening or serious medical condition, such as severe renal, hepatic, and cardiovascular disease, which would prevent completion of the study protocol, impair the assessment of outcome, or in which sovateltide therapy would be contraindicated or might cause harm to the participant.
  9. Concurrent participation in any other therapeutic clinical trial.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:四人间

武器和干预

参与者组/臂
干预/治疗
安慰剂比较:The reference product is a matching placebo for sovateltide

The reference product is a matching placebo for sovateltide. It is a sterile lyophilized injection consisting of excipients formulated without the active ingredient in a 5.0 mL vial, to be reconstituted in 5 mL of normal saline (0.9% Sodium Chloride Injection).

有源比较器:The test product is sovateltide

The test product is sovateltide. It is available as a lyophilized injection containing 30 μg of sovateltide in a 5.0 mL vial, to be reconstituted in 5 mL normal saline (0.9% Sodium Chloride Injection).

其他名称:
  • IRL-1620

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Proportion of patients achieving a favorable functional outcome (GOS-E score ≥7) at Day 90 post-randomization. Score range: 1 to 8; higher scores represent a better outcome.
大体时间:90 days

Score Range: 1 to 8 (minimum: 1, maximum: 8); Direction of Score: Higher scores represent a better outcome (1 indicates Death; 7 indicates Lower Good Recovery; 8 indicates Upper Good Recovery).

90 days

次要结果测量

结果测量
措施说明
大体时间
Proportion of patients achieving a favorable functional outcome (GOS-E score ≥7) at Day 180 post-randomization. Score range: 1 to 8; higher scores represent a better outcome.
大体时间:180 days

Score Range: 1 to 8 (minimum: 1, maximum: 8); Direction of Score: Higher scores represent a better outcome (1 indicates Death; 7 indicates Lower Good Recovery; 8 indicates Upper Good Recovery).

180 days
Proportion of patients achieving a favorable functional outcome (GOS-E score ≥7) at Day 30 post-randomization. Score range: 1 to 8; higher scores represent a better outcome.
大体时间:30 days

Score Range: 1 to 8 (minimum: 1, maximum: 8); Direction of Score: Higher scores represent a better outcome (1 indicates Death; 7 indicates Lower Good Recovery; 8 indicates Upper Good Recovery).

30 days
Proportion of patients with an improvement in Disability Rating Scale (DRS) to less than or equal to 3 at Days 30, 90, and 180 post randomization. Score range: 0 to 30; higher scores represent a worse outcome.
大体时间:180 days

Score Range: 0 to 30 (minimum: 0, maximum: 30); Direction of Score: Higher scores represent a worse outcome (0 indicates no disability; 30 indicates death).

180 days
Change in the Montreal Cognitive Assessment (MoCA) at Days 30, 90, and 180 post-randomization. Score range: 0 to 30; higher scores represent a better outcome.
大体时间:180 days

Score Range: 0 to 30 (minimum: 0, maximum: 30); Direction of Score: Higher scores represent a better outcome (scores of 26 and above are generally considered normal cognitive function; lower scores indicate greater cognitive impairment).

180 days
Change in the quality-of-life outcomes using Short Form (36) Health Survey (SF-36) at Days 30, 60, 90, 135, and 180 post-randomization.
大体时间:180 days
180 days
Hospital free days from randomization to Day 90.
大体时间:90 days
90 days
ICU free days from randomization to Day 90.
大体时间:90 days
90 days
Incidence of all-cause mortality from randomization to Day 180.
大体时间:180 days
180 days
Proportion of patients with adverse events (AEs) and serious adverse events (SAEs).
大体时间:180 days
180 days

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年12月1日

初级完成 (估计的)

2028年2月1日

研究完成 (估计的)

2028年3月1日

研究注册日期

首次提交

2026年9月30日

首先提交符合 QC 标准的

2026年9月30日

首次发布 (实际的)

2026年10月6日

研究记录更新

最后更新发布 (实际的)

2026年10月13日

上次提交的符合 QC 标准的更新

2026年10月7日

最后验证

2026年10月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 共享支持信息类型

  • 研究方案

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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