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Protagenic Therapeutics Successfully Concludes Third Cohort in Single Dose Portion of Phase 1 Trial for Stress-Related Neuropsychiatric Disorders

Protagenic Therapeutics Successfully Concludes Third Cohort in Single Dose Portion of Phase 1 Trial for Stress-Related Neuropsychiatric Disorders

Protagenic Therapeutics成功完成了压力相关神经精神疾病1期试验单剂量部分的第三组队列
Accesswire ·  03/27 08:42

Next clinical progress update expected in April 2024

下一次临床进展更新预计将于2024年4月发布

NEW YORK, NY / ACCESSWIRE / March 27, 2024 / Protagenic Therapeutics, Inc. (NASDAQ:PTIX), a leader in biopharmaceutical innovation, advances its mission to develop cutting-edge treatments for stress-related neuropsychiatric disorders. The company has reached another milestone by completing three out of five cohorts of healthy volunteers with PT00114, its synthetic version of the stress-regulating peptide TCAP, in a SAD Phase 1 clinical trial. Notably, PT00114 has shown excellent tolerability with no adverse safety findings during these ongoing Phase 1 studies. With promising preclinical efficacy in anxiety, depression, PTSD, and addiction models, PT00114 moves forward in clinical evaluation, representing a step toward potentially transformative therapies.

纽约州纽约/ACCESSWIRE/2024年3月27日/生物制药创新的领导者Protagenic Therapeutics, Inc.(纳斯达克股票代码:PTIX)推进了为压力相关的神经精神疾病开发尖端疗法的使命。该公司在一项SAD 1期临床试验中完成了五分之三的健康志愿者队列使用其压力调节肽TCAP的合成版本 PT00114,从而实现了又一个里程碑。值得注意的是,在这些正在进行的 1 期研究中,PT00114 表现出良好的耐受性,没有不良的安全性发现。PT00114 在焦虑、抑郁、创伤后应激障碍和成瘾模型中的临床前疗效令人鼓舞,临床评估向前迈进,标志着朝着潜在的变革性疗法迈出了一步。

Key Highlights:

主要亮点:

  • Safety Validation: Building on the low dose safety validation announced February 13th, PT00114 has now demonstrated safety at a medium dose of 500 micrograms administered subcutaneously in the third of five planned cohorts of subjects in the single dose portion of the Phase I trial. No adverse reactions were observed among subjects, consistent with the two lower dose cohorts (125 micrograms and 250 micrograms), with no reported injection site reactions or tolerability issues in the week following dosing. Based on preclinical pharmacology, PT00114 is expected to be administered once weekly via subcutaneous injection.
  • Clinical Protocol Progress: This marks progress in the ongoing Phase 1/2a trial, designed to assess both healthy volunteers and patients diagnosed with Treatment-Resistant Depression, PTSD, or Generalized Anxiety Disorder. The company plans to enroll the final two cohorts into the single dose portion of the Phase 1 trial within the next month.
  • Comprehensive Approach: In addition to monitoring disease status, the trial incorporates biomarker assessments, including circulating cortisol levels, to measure initial treatment response. Dr. Maurizio Fava, Psychiatrist-in-Chief at Massachusetts General Hospital, serves as the Principal Investigator in Protagenic's Phase 1/2a clinical trial with a basket design.
  • Strategic Collaboration: Axiom Real-Time Metrics, a CRO/Data Analytics firm, manages the clinical program.
  • 安全性验证:在 2 月 13 日宣布的低剂量安全性验证基础上,PT00114 现已证明在 I 期试验单剂量部分计划中的五组受试者中进行皮下给药 500 微克的中等剂量是安全的。受试者中未观察到不良反应,这与两个较低剂量的队列(125微克和250微克)一致,在给药后的一周内没有报告注射部位反应或耐受性问题。根据临床前药理学,PT00114 预计将通过皮下注射每周给药一次。
  • 临床方案进展:这标志着正在进行的1/2a期试验的进展,该试验旨在评估健康志愿者和被诊断患有耐药性抑郁症、创伤后应激障碍或广泛性焦虑症的患者。该公司计划在下个月内将最后两个队列纳入1期试验的单剂量部分。
  • 综合方法:除了监测疾病状况外,该试验还包括生物标志物评估,包括循环皮质醇水平,以衡量初始治疗反应。麻省总医院首席精神科医生毛里齐奥·法瓦博士是Protagenic采用篮子设计的1/2a期临床试验的首席研究员。
  • 战略合作:首席投资官/数据分析公司Axiom Real-time Metrics负责管理临床项目。

About Protagenic Therapeutics, Inc.:
Protagenic Therapeutics, Inc. (Nasdaq: PTIX) is dedicated to pioneering therapeutics based on neuro-active peptides to alleviate the negative effects of stress and treat stress-related disorders such as anxiety, depression, PTSD, and addiction. For more information, visit .

关于 Protagenic Therapeutics, Inc.:
Protagenic Therapeutics, Inc.(纳斯达克股票代码:PTIX)致力于开发基于神经活性肽的开创性疗法,以减轻压力的负面影响并治疗与压力相关的疾病,例如焦虑、抑郁、创伤后应激障碍和成瘾。欲了解更多信息,请访问。

About PT00114:
PT00114, a 41-amino-acid residue synthetic peptide, shows promise as a novel treatment for serious neuro-psychiatric conditions, including depression, anxiety, and PTSD. It is a synthetic form of the naturally occurring brain peptide TCAP, which counters the negative biochemical and behavioral effects of stress-induced brain hormones Corticotropin Releasing Factor and Arginine-Vasopressin. Among its benefits is the reduction of excessive circulating levels of cortisol often associated with various stressors.

关于 PT00114:
PT00114 是一种 41 氨基酸残留的合成肽,有望成为严重神经精神疾病(包括抑郁、焦虑和创伤后应激障碍)的新疗法。它是天然存在的大脑肽 TCAP 的合成形式,可抵消压力诱导的大脑激素促肾上腺激素促肾上腺皮质激素释放因子和精氨酸加压素的负面生化和行为影响。它的好处之一是降低了皮质醇的过高循环水平,通常与各种压力有关。

Forward-Looking Statements:
This press release contains forward-looking statements concerning Protagenic Therapeutics' product candidates and clinical trial plans. These statements are subject to various risks and uncertainties. Investors are urged to exercise caution and not place undue reliance on these forward-looking statements.

前瞻性陈述:
本新闻稿包含有关Protagenic Therapeutics候选产品和临床试验计划的前瞻性陈述。这些陈述受各种风险和不确定性的影响。敦促投资者谨慎行事,不要过分依赖这些前瞻性陈述。

Company Contact:
Alexander K. Arrow, MD, CFA
Chief Financial Officer
Protagenic Therapeutics, Inc. 149 Fifth Ave, Suite 500, New York, NY 10010. Tel: 213-260-4342
Email: alex.arrow@protagenic.com

公司联系人:
亚历山大·阿罗,医学博士,特许金融分析师
首席财务官
Protagenic Therapeutics, Inc. 第五大道 149 号,套房 500,纽约,纽约州 10010。电话:213-260-4342
电子邮件:alex.arrow@protagenic.com

Investor Relations Contact:
Kirin M. Smith, President, PCG Advisory, Inc. 950 Third Avenue, Suite #2700, New York, NY 10022. Tel: 646-823-8656 Email: ksmith@pcgadvisory.com

投资者关系联系人:
Kirin M. Smith,PCG Advisory, Inc. 总裁。第三大道950号,套房 #2700,纽约,纽约州,10022。电话:646-823-8656 电子邮件:ksmith@pcgadvisory.com

SOURCE: Protagenic Therapeutics, Inc.

来源:Protagenic Therapeutics, Inc.


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