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Tectonic Therapeutic to Host KOL Event on the Unmet Need in Group 2 PH-HFpEF and TX45 as a Potential Treatment on Thursday, December 12, 2024

Tectonic Therapeutic to Host KOL Event on the Unmet Need in Group 2 PH-HFpEF and TX45 as a Potential Treatment on Thursday, December 12, 2024

Tectonic Therapeutic將於2024年12月12日星期四舉辦關於2型PH-HFpEF領域未滿足需求及TX45作爲潛在治療方案的KOL活動。
GlobeNewswire ·  12/04 05:01

WATERTOWN, Mass., Dec. 03, 2024 (GLOBE NEWSWIRE) -- Tectonic Therapeutic, Inc. (NASDAQ: TECX) ("Tectonic") a clinical stage biotechnology company focused on the discovery and development of therapeutic proteins and antibodies that modulate the activity of G-protein coupled receptors ("GPCRs"), today announced it will host a virtual key opinion leader (KOL) event on Thursday, December 12, 2024 from 4:00 PM to 6:00 PM ET. To register, click here.

馬薩諸塞州沃特敦,2024年12月03日(環球新聞) -- 特考尼克治療公司。 (納斯達克:TECX)("Tectonic")是一家處於臨床階段的生物技術公司,專注於發現和開發能夠調節G蛋白偶聯受體("GPCRs")活性的治療性蛋白和抗體,今天宣佈將於2024年12月12日(星期四)東部時間下午4:00至下午6:00舉辦一次虛擬的關鍵意見領袖(KOL)活動。要註冊, 點擊這裏.

Key opinion leaders will include John R. Teerlink, MD, FHFSA (University of California San Francisco) and Raymond L. Benza, MD, FACC, FAHA, FACP (Icahn School of Medicine at Mount Sinai), who will discuss the unmet medical need and current treatment landscape for patients with Group 2 Pulmonary Hypertension due to Heart Failure with Preserved Ejection Fraction (Group 2 PH-HFpEF).

關鍵意見領袖將包括約翰·R·蒂爾林克醫學博士(加利福尼亞大學舊金山分校)和雷蒙德·L·本扎醫學博士(西奈山醫學院),他們將討論心衰伴保留射血分數的2組肺動脈高壓患者的未滿足醫療需求和當前治療情況(2組PH-HFpEF)。

The event will focus on Tectonic's lead program, TX45, an investigational Fc-relaxin fusion protein with optimized pharmacokinetics and biophysical properties that activates the RXFP1 receptor, the GPCR target of the hormone relaxin. TX45 is being evaluated in patients with Group 2 PH-HFpEF in an ongoing Phase 1b hemodynamic proof-of-concept study and a Phase 2 clinical proof-of-concept study.

該活動將重點關注Tectonic的領先項目TX45,這是一種研究性Fc-relaxin融合蛋白,具有優化的藥物代謝動力學和生物物理特性,能夠激活RXFP1受體,這是黃體酮的GPCR靶點。TX45正在一項正在進行的10億相位血流動力學概念驗證研究和一項第二階段臨床概念驗證研究中評估2組PH-HFpEF患者。

A live question and answer session will follow the formal presentations.

正式發言後將進行互動問答環節。

About the Key Opinion Leaders:

關於主要意見領袖:

Professor John R. Teerlink, MD, FACC, FAHA, FESC, FHFA, FHFSA, FRCP (London)
Professor Teerlink is Professor of Medicine at the University of California San Francisco (UCSF). After graduating from Swarthmore College with a Religion major, he received an MD from Harvard Medical School and completed his Internal Medicine residency and Cardiovascular Medicine fellowship at UCSF, as well as post-doctoral fellowships in Cardiovascular pharmacology (Hoffman-LaRoche; Basel, Switzerland), echocardiography (UCSF) and heart failure (UCSF-affiliated hospital).

約翰·R·特爾林克教授,醫學博士,FACC,FAHA,FESC,FHFA,FHFSA,FRCP(倫敦)
特爾林克教授是加利福尼亞大學舊金山分校(UCSF)的醫學教授。在斯沃斯莫爾學院獲得宗教專業學位後,他獲得了哈佛醫學院的醫學博士學位,並在UCSF完成了內科住院醫師和心血管醫學的專科培訓,以及在心血管藥理學(霍夫曼-拉羅氏;瑞士巴塞爾)、超聲心動圖(UCSF)和心力衰竭(UCSF附屬醫院)的博士後研究。

He is actively involved in the design and execution of many heart failure clinical trials, serving on endpoint, data monitoring, steering and executive committees for numerous international studies investigating a variety of new pharmacologic therapies, as well as stem cell and gene therapies, diagnostic modalities and other devices. He was the lead clinical investigator for the serelaxin development program, serving as Principal Investigator for Pre-RELAX-AHF, RELAX-AHF, RELAX-AHF-2 and RELAX-Repeat, and as a steering committee member for RELAX-AHF-Asia.

他積極參與許多心力衰竭臨床試驗的設計和實施,擔任多個國際研究的終點、數據監測、指導和執行委員會成員,研究各種新的藥物療法,以及幹細胞和基因療法、診斷方式和其他設備。他是serelaxin開發項目的首席臨床研究員,擔任Pre-RELAX-AHF、RELAX-AHF、RELAX-AHF-2和RELAX-Repeat的主要研究員,同時是RELAX-AHF-Asia的指導委員會成員。

Dr. Teerlink has served on the US FDA Cardiovascular and Renal Drug Advisory Committee, as well as on other FDA drug, device, diagnostics, and vaccine panels and serves as a consultant on pre-clinical and clinical development programs in multiple areas of cardiology, as well as in non-cardiovascular indications. Dr. Teerlink was a founding physician member of the American Association of Heart Failure Nurses and is a Past President of the Heart Failure Society of America. He was an Associate Editor for the Journal of Cardiac Failure, Guest Editor-in-Chief and Associate Editor for JACC: Heart Failure, and is a clinical scholar presenting many lectures and over 300 publications, including a chapter on Acute Heart Failure in Braunwald's Heart Disease textbook. He was profiled in The Lancet as an internationally recognized leader in heart failure.

Teerlink博士曾擔任美國FDA心血管和腎臟藥物顧問委員會成員,以及其他FDA藥物、設備、診斷和疫苗小組的成員,並在多個心臟病領域的前臨床和臨床開發項目中擔任顧問。Teerlink博士是美國心力衰竭護理協會的創始醫師成員,並曾擔任美國心力衰竭學會的前任主席。他曾是《心臟衰竭雜誌》的副編輯,《JACC: 心力衰竭》的特邀主編和副編輯,並是一位臨床學者,發表了許多講座和超過300篇出版物,包括Braunwald心臟病教科書中的急性心力衰竭一章。他在《柳葉刀》上被評爲國際公認的心力衰竭領導者。

Raymond L. Benza, MD, FACC, FAHA, FACP
Dr. Benza is a Professor and System Director of Pulmonary Hypertension at the Icahn School of Medicine at Mount Sinai, Mount Sinai Fuster Heart Hospital. He is a fellow of the American College of Physicians, the American Heart Association Council on Clinical Cardiology, the American College of Chest Physicians and the American College of Cardiology. He is a diplomat of the American Board of Internal Medicine with certification in the subspecialties of cardiovascular diseases and advanced heart failure and transplantation. Dr. Benza currently holds administrative positions in the Pulmonary Vascular Research Institute and the International Society of Heart and Lung Transplantation and is the former treasurer of that society. He served on President Barak Obama's Advisory Committee on Organ Transplantation (ACOT) in the Health Resources and Services Administration for 4 years and was knighted in 2015 by his Royal Highness Vittorio Emanuele of Italy for his philanthropic work in patients with pulmonary arterial hypertension and was admitted to the Association of University Cardiologists. He sits on multiple journal editorial committees and is the Steering Committee Chair for several industry trials in PAH. His primary clinical interests are the evaluation and treatment of advanced congestive heart failure, cardiac transplantation, and pulmonary arterial hypertension (PAH). He participates in major clinical studies of new therapies for the treatment of heart failure, mechanical support, and pulmonary hypertension. Dr. Benza is a funded investigator for the National Institutes of Health and the American Heart Association for his work in pulmonary arterial hypertension focusing on risk stratification, pharmacogenomics and new device therapies for this disease state.

雷蒙德·L·本扎,醫學博士,FACC,FAHA,FACP
本扎博士是愛坎醫學院肺動脈高壓系統主任教授,位於西奈山Mount Sinai Fuster心臟醫院。他是美國內科醫師學會、美國心臟協會臨床心臟病委員會、美國胸科醫師學會和美國心臟病學會的會員。他是美國內科學委員會的文憑持有者,具有心血管疾病及高級心力衰竭和移植的子專業認證。本扎博士目前在肺血管研究院和國際心肺移植學會擔任行政職務,並曾是該學會的財務主管。他在健康資源和服務管理局的奧巴馬總統組織移植顧問委員會(ACOT)中工作了4年,並因其對肺動脈高壓患者的慈善工作於2015年被意大利維托里奧·埃馬努埃爾王子封爲騎士,並被接納爲大學心臟病學家協會成員。他在多個期刊編輯委員會任職,並擔任多個肺動脈高壓行業試驗的指導委員會主席。他的主要臨床興趣是晚期充血性心力衰竭、心臟移植和肺動脈高壓(PAH)的評估和治療。他參與了心力衰竭、新療法、機械支持和肺動脈高壓的重大臨床研究。本扎博士是國家衛生研究院和美國心臟協會的資助研究員,專注於肺動脈高壓的風險分層、藥物基因組學和這一疾病狀態的新設備療法的研究。

About TX45, a long-acting Fc-relaxin fusion protein
TX45 is an investigational Fc-relaxin fusion protein with optimized pharmacokinetics and biophysical properties that activates the RXFP1 receptor, the G-protein coupled receptor target of the hormone relaxin. Relaxin is an endogenous protein, expressed at low levels in both men and women that is a pulmonary and systemic vasodilator with lusitropic, anti-fibrotic and anti-inflammatory activity. In normal human physiology, relaxin is upregulated during pregnancy where it exerts vasodilative effects, reduces systemic and pulmonary vascular resistance and increases cardiac output to accommodate the increased demand for oxygen and nutrients from the developing fetus. Relaxin also exerts anti-fibrotic effects on pelvic ligaments to facilitate delivery of the baby.

關於TX45,這是一種長效Fc-relaxin融合蛋白
TX45 is an investigational Fc-relaxin fusion protein with optimized pharmacokinetics and biophysical properties that activates the RXFP1 receptor, the G-protein coupled receptor target of the hormone relaxin. Relaxin is an endogenous protein, expressed at low levels in both men and women that is a pulmonary and systemic vasodilator with lusitropic, anti-fibrotic and anti-inflammatory activity. In normal human physiology, relaxin is upregulated during pregnancy where it exerts vasodilative effects, reduces systemic and pulmonary vascular resistance and increases cardiac output to accommodate the increased demand for oxygen and nutrients from the developing fetus. Relaxin also exerts anti-fibrotic effects on pelvic ligaments to facilitate delivery of the baby.

About Group 2 Pulmonary Hypertension in HFpEF
The World Health Organization has defined five groups of pulmonary hypertension ("PH"). Tectonic is focused on the Group 2 subtype, a condition that develops due to left-sided heart disease, specifically pulmonary hypertension secondary to left heart failure with preserved ejection fraction ("PH-HFpEF"). In patients with PH-HFpEF, chronic heart failure leads to increased blood pressure in the pulmonary arteries, exerting severe strain on the right side of the heart, which adapts poorly to the increased pressure. This increased pulmonary pressure gradually causes worsening exercise capacity, shortness of breath and right-sided heart failure which can lead to death. Although several Group 1 PH (Pulmonary Arterial Hypertension, PAH) medications have been explored in Group 2 PH, to date, no medications have been approved for its treatment.

關於2組HFpEF的肺動脈高壓
The World Health Organization has defined five groups of pulmonary hypertension ("PH"). Tectonic is focused on the Group 2 subtype, a condition that develops due to left-sided heart disease, specifically pulmonary hypertension secondary to left heart failure with preserved ejection fraction ("PH-HFpEF"). In patients with PH-HFpEF, chronic heart failure leads to increased blood pressure in the pulmonary arteries, exerting severe strain on the right side of the heart, which adapts poorly to the increased pressure. This increased pulmonary pressure gradually causes worsening exercise capacity, shortness of breath and right-sided heart failure which can lead to death. Although several Group 1 PH (Pulmonary Arterial Hypertension, PAH) medications have been explored in Group 2 PH, to date, no medications have been approved for its treatment.

About Tectonic
Tectonic is a biotechnology company focused on the discovery and development of therapeutic proteins and antibodies that modulate the activity of G-protein coupled receptors ("GPCRs"). Leveraging its proprietary technology platform called GEODe (GPCRs Engineered for Optimal Discovery), Tectonic is focused on developing biologic medicines that overcome the existing challenges of GPCR-targeted drug discovery and harness the human body to modify the course of disease. Tectonic focuses on areas of significant unmet medical need, often where therapeutic options are poor or nonexistent, as these are areas where new medicines have the potential to improve patient quality of life. Tectonic is headquartered in Watertown, Massachusetts. For more information, please visit and follow on LinkedIn.

關於Tectonic
Tectonic is a biotechnology company focused on the discovery and development of therapeutic proteins and antibodies that modulate the activity of G-protein coupled receptors ("GPCRs"). Leveraging its proprietary technology platform called GEODe (GPCRs Engineered for Optimal Discovery), Tectonic is focused on developing biologic medicines that overcome the existing challenges of GPCR-targeted drug discovery and harness the human body to modify the course of disease. Tectonic focuses on areas of significant unmet medical need, often where therapeutic options are poor or nonexistent, as these are areas where new medicines have the potential to improve patient quality of life. Tectonic is headquartered in Watertown, Massachusetts. For more information, please visit 並在之後關注LinkedIn.

Forward-Looking Statements
This press release contains "forward-looking statements" within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. All statements in this press release other than statements of historical facts are "forward-looking statements. These statements may be identified by words such as "aims," "anticipates," "believes," "could," "estimates," "expects," "forecasts," "goal," "intends," "may," "plans," "possible," "potential," "seeks," "will" and variations of these words or similar expressions that are intended to identify forward-looking statements, although not all forward-looking statements contain these words. Forward-looking statements in this press release include statements regarding: the design, objectives, initiation, timing, progress and results of clinical trials of Tectonic's product candidates, including the ongoing Phase 1b and Phase 2 clinical trials for TX45 in Group 2 PH-HFpEF; and the potential properties and benefits of TX45. These forward-looking statements are based on Tectonic's expectations and assumptions as of the date of this press release. Each of these forward-looking statements involves risks and uncertainties that could cause Tectonic's clinical development programs, future results or performance to differ materially from those expressed or implied by the forward-looking statements. Many factors may cause differences between current expectations and actual results, including: the potential that success in preclinical testing and earlier clinical trials does not ensure that later clinical trials will generate the same results or otherwise provide adequate data to demonstrate the efficacy and safety of a product candidate; the impacts of macroeconomic conditions, including the conflict in Ukraine and the conflict in the Middle East, heightened inflation and uncertain credit and financial markets, on Tectonic's business, clinical trials and financial position; unexpected safety or efficacy data observed during preclinical studies or clinical trials; clinical trial site activation or enrollment rates that are lower than expected; Tectonic's ability to realize the benefits of its collaborations and license agreements; changes in expected or existing competition; changes in the regulatory environment; the uncertainties and timing of the regulatory approval process; and unexpected litigation or other disputes. Other factors that may cause Tectonic's actual results to differ from those expressed or implied in the forward-looking statements in this press release are identified under the heading "Risk Factors" in Tectonic's quarterly report on Form 10-Q filed with the SEC on November 12, 2024, and in other filings that Tectonic makes and will make with the SEC in the future. Tectonic expressly disclaims any obligation to update any forward-looking statements contained herein, whether as a result of any new information, future events, changed circumstances or otherwise, except as otherwise required by law. For more information, please visit and follow on LinkedIn.

前瞻性聲明
This press release contains "forward-looking statements" within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. All statements in this press release other than statements of historical facts are "forward-looking statements. These statements may be identified by words such as "aims," "anticipates," "believes," "could," "estimates," "expects," "forecasts," "goal," "intends," "may," "plans," "possible," "potential," "seeks," "will" and variations of these words or similar expressions that are intended to identify forward-looking statements, although not all forward-looking statements contain these words. Forward-looking statements in this press release include statements regarding: the design, objectives, initiation, timing, progress and results of clinical trials of Tectonic's product candidates, including the ongoing Phase 10億 and Phase 2 clinical trials for TX45 in Group 2 PH-HFpEF; and the potential properties and benefits of TX45. These forward-looking statements are based on Tectonic's expectations and assumptions as of the date of this press release. Each of these forward-looking statements involves risks and uncertainties that could cause Tectonic's clinical development programs, future results or performance to differ materially from those expressed or implied by the forward-looking statements. Many factors may cause differences between current expectations and actual results, including: the potential that success in preclinical testing and earlier clinical trials does not ensure that later clinical trials will generate the same results or otherwise provide adequate data to demonstrate the efficacy and safety of a product candidate; the impacts of macroeconomic conditions, including the conflict in Ukraine and the conflict in the Middle East, heightened inflation and uncertain credit and financial markets, on Tectonic's business, clinical trials and financial position; unexpected safety or efficacy data observed during preclinical studies or clinical trials; clinical trial site activation or enrollment rates that are lower than expected; Tectonic's ability to realize the benefits of its collaborations and license agreements; changes in expected or existing competition; changes in the regulatory environment; the uncertainties and timing of the regulatory approval process; and unexpected litigation or other disputes. Other factors that may cause Tectonic's actual results to differ from those expressed or implied in the forward-looking statements in this press release are identified under the heading "Risk Factors" in Tectonic's quarterly report on Form 10-Q filed with the SEC on November 12, 2024, and in other filings that Tectonic makes and will make with the SEC in the future. Tectonic expressly disclaims any obligation to update any forward-looking statements contained herein, whether as a result of any new information, future events, changed circumstances or otherwise, except as otherwise required by law. For more information, please visit 並在之後關注LinkedIn.

Source: Tectonic Therapeutic

來源:Tectonic Therapeutic

CONTACT: Contacts:

Investors:
Dan Ferry
LifeSci Advisors
(617) 430-7576
daniel@lifesciadvisors.com

Media:
Kathryn Morris
The Yates Network
(914) 204-6412
kathryn@theyatesnetwork.com
Investors: investor@enthusiastgaming.com

投資者:
丹·費裏,電話:(617) 430-7576
LifeSci顧問
(617) 430-7576
daniel@lifesciadvisors.com

媒體:
Kathryn Morris
耶茨網絡
(914) 204-6412
kathryn@theyatesnetwork.com

譯文內容由第三人軟體翻譯。


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