A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Dose Finding Study to Assess the Safety and Effectiveness of Tovinontrine in Patients With Chronic Heart Failure With Reduced Ejection Fraction - CRD-750-201

开始日期2024-08-19

申办/合作机构

Cardurion Pharmaceuticals, Inc.

NCT06215911

/ Active, not recruiting临床2期

The purpose of this study is to evaluate the safety and effectiveness of tovinontrine compared to placebo to lower NT-proBNP in patients with chronic heart failure with reduced ejection fraction.

开始日期2024-02-13

申办/合作机构

Cardurion Pharmaceuticals, Inc.

NCT06215586

/ Completed临床2期

A Phase 2, Randomized, Double-Blind, Placebo-Controlled Clinical Study to Assess the Safety and Effectiveness of Tovinontrine in Patients With Chronic Heart Failure With Preserved Ejection Fraction

The purpose of this study is to evaluate the safety and effectiveness of tovinontrine compared to placebo to lower NT-proBNP in patients with chronic heart failure with preserved ejection fraction

开始日期2024-02-13

申办/合作机构

Cardurion Pharmaceuticals, Inc.

100 项与 Tovinontrine 相关的临床结果

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100 项与 Tovinontrine 相关的转化医学

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100 项与 Tovinontrine 相关的专利（医药）

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项与 Tovinontrine 相关的文献（医药）

2021-12-10·Hematology. American Society of Hematology. Education Program3区 · 教育学

β-Thalassemia: evolving treatment options beyond transfusion and iron chelation

3区 · 教育学

Review

作者: Langer, Arielle L. ; Esrick, Erica B.

Abstract:

After years of reliance on transfusion alone to address anemia and suppress ineffective erythropoiesis in β-thalassemia, many new therapies are now in development. Luspatercept, a transforming growth factor–β inhibitor, has demonstrated efficacy in reducing ineffective erythropoiesis, improving anemia, and possibly reducing iron loading. However, many patients do not respond to luspatercept, so additional therapeutics are needed. Several medications in development aim to induce hemoglobin F (HbF): sirolimus, benserazide, and IMR-687 (a phosphodiesterase 9 inhibitor). Another group of agents seeks to ameliorate ineffective erythropoiesis and improve anemia by targeting abnormal iron metabolism in thalassemia: apotransferrin, VIT-2763 (a ferroportin inhibitor), PTG-300 (a hepcidin mimetic), and an erythroferrone antibody in early development. Mitapivat, a pyruvate kinase activator, represents a unique mechanism to mitigate ineffective erythropoiesis. Genetically modified autologous hematopoietic stem cell transplantation offers the potential for lifelong transfusion independence. Through a gene addition approach, lentiviral vectors have been used to introduce a β-globin gene into autologous hematopoietic stem cells. One such product, betibeglogene autotemcel (beti-cel), has reached phase 3 trials with promising results. In addition, 2 gene editing techniques (CRISPR-Cas9 and zinc-finger nucleases) are under investigation as a means to silence BCL11A to induce HbF with agents designated CTX001 and ST-400, respectively. Results from the many clinical trials for these agents will yield results in the next few years, which may end the era of relying on transfusion alone as the mainstay of thalassemia therapy.

2021-08-01·American journal of hematology

SARS‐CoV‐2 infection in patients with β‐thalassemia: Experience from Lebanon

Letter

作者: Noun, Peter ; Bou‐Fakhredin, Rayan ; Abou Nasr, Therese ; Koussa, Suzanne ; Taher, Ali T. ; Daadaa, Hisham

In this report, severity of Covid-19 was investigated among β-thalassemia patients who are regularly followed up at the Chronic Care Center (CCC), tertiary care thalassemia center in Lebanon.Patients' clin. characteristics, Covid-19 signs and symptoms, treatment, disease course and outcomes were collected by analyzing patients' medical records and by directly calling the patients and checking on their well-being.The comorbidities present among our β-thalassemia patients are reported in the Table S1.Overall, 37 (92.5%) patients had at least one comorbidity. Most of our patients suffered from iron overload.Liver iron concentration (LIC) (mg/g) was classified as: mild (LIC 3-7 mg/g), moderate (LIC >7-14 mg/g), and severe overload (LIC >15 mg/g).In our patient cohort 13 (32.5%) patients had mild iron overload, seven (20.6%) patients had moderate iron overload, and six (17.6%) patient had severe iron overload. Eight patients never had their LIC determinedTwenty six patients (65%) were splenectomized.Of the 26 splenectomized patients, 19/26 (73.1%) were on aspirin, 1/26 (3.8%) was on warfarin for his co-existing atrial fibrillation, and 3/26 (11.5%) were switched to low mol. weight heparin (enoxaparin) in the hospital setting.

2020-03-01·Haematologica1区 · 医学

A novel, highly potent and selective phosphodiesterase-9 inhibitor for the treatment of sickle cell disease

1区 · 医学

Article

作者: Nguyen, Phong ; Belcher, John D ; Ribeil, Jean-Antoine ; McArthur, James G ; Abdulla, Fuad ; Nguyen, Julia ; Edwards, Dave ; Fricot, Aurelie ; Hermine, Olivier ; Chen, Chunsheng ; Parachikova, Anna ; Maciel, Thiago T ; Svenstrup, Niels ; Vercellotti, Gregory M ; Carvalho, Caroline

The most common treatment for patients with sickle cell disease (SCD) is the chemotherapeutic hydroxyurea, a therapy with pleiotropic effects, including increasing fetal hemoglobin (HbF) in red blood cells and reducing adhesion of white blood cells to the vascular endothelium. Hydroxyurea has been proposed to mediate these effects through a mechanism of increasing cellular cGMP levels. An alternative path to increasing cGMP levels in these cells is through the use of phosphodiesterase-9 inhibitors that selectively inhibit cGMP hydrolysis and increase cellular cGMP levels. We have developed a novel, potent and selective phosphodiesterase-9 inhibitor (IMR-687) specifically for the treatment of SCD. IMR-687 increased cGMP and HbF in erythroid K562 and UT-7 cells and increased the percentage of HbF positive erythroid cells generated in vitro using a two-phase liquid culture of CD34⁺ progenitors from sickle cell blood or bone marrow. Oral daily dosing of IMR-687 in the Townes transgenic mouse SCD model, increased HbF and reduced red blood cell sickling, immune cell activation and microvascular stasis. The IMR-687 reduction in red blood cell sickling and immune cell activation was greater than that seen with physiological doses of hydroxyurea. In contrast to other described phosphodiesterase-9 inhibitors, IMR-687 did not accumulate in the central nervous system, where it would inhibit phosphodiesterase-9 in neurons, or alter rodent behavior. IMR-687 was not genotoxic or myelotoxic and did not impact fertility or fetal development in rodents. These data suggest that IMR-687 may offer a safe and effective oral alternative for hydroxyurea in the treatment of SCD.

项与 Tovinontrine 相关的新闻（医药）

2025-08-08

·GlobeNewswire-Health Care

Cardurion Pharmaceuticals Completes Enrollment in Phase 2 CYCLE Trials Evaluating CRD-750, a Novel PDE9 inhibitor, in Heart Failure

CRD-750 is the first clinical-stage PDE9 inhibitor to be evaluated in patients in both types of chronic heart failure The CYCLE-1-REF trial is evaluating patients with heart failure with reduced ejection fraction (HFrEF), and the CYCLE-2-PEF trial is evaluating patients with heart failure with preserved ejection fraction (HFpEF) Aug. 06, 2025 -- Cardurion Pharmaceuticals, Inc. (“Cardurion”), a clinical-stage biotechnology company discovering and developing new therapeutic approaches for the treatment of patients with cardiovascular diseases, today announced that it has completed enrollment in two global, multi-center, Phase 2 clinical trials assessing the safety and efficacy of CRD-750 in both types of chronic heart failure (HFrEF and HFpEF). CRD-750 is an orally-administered phosphodiesterase 9 (PDE9) inhibitor that represents a new mechanism to enhance the natriuretic peptide signaling (NPS) pathway, a clinically-validated pathway for the treatment of patients with heart failure. Cardurion is the first company to bring a PDE9 inhibitor into clinical development for the treatment of chronic heart failure. The CYCLE-1-REF trial (NCT06215911) enrolled approximately 560 patients with HFrEF and is evaluating three doses of CRD-750 compared to placebo. CYCLE-2-PEF (NCT06215586) enrolled approximately 300 patients with HFpEF and is evaluating one dose of CRD-750 compared to placebo. The primary endpoint of both CYCLE clinical trials is the change in N-terminal pro-B-type natriuretic peptide (NT-proBNP), a peptide that is released by the heart in the setting of heart failure. Reduction in NT-proBNP has been used as a biomarker to measure the treatment effect in clinical trials of other approved heart failure therapies. The trials are also evaluating secondary endpoints, including additional biomarkers and the Kansas City Cardiomyopathy Questionnaire (KCCQ), a patient-reported outcomes scale. “The clinical community eagerly awaits the results of the CYCLE clinical trials. Despite recent approvals, a large unmet medical need persists and patients with heart failure continue to experience high rates of morbidity and mortality. PDE9 inhibition is a promising new mechanism in the NPS pathway that may offer an opportunity to improve the standard of care treatment for the millions of patients with both types of chronic heart failure,” said James Udelson, MD, Chief of Cardiology at Tufts Medical Center and Principal Investigator for the CYCLE-1-REF and CYCLE-2-PEF trials. “Completion of enrollment in the CYCLE trials represents a major milestone in our CRD-750 clinical program. Since the founding of Cardurion, our team has believed that the upregulation of PDE9 that occurs in heart failure is a critical element limiting the beneficial clinical effects of the highly validated NPS pathway. Our progress brings us closer to our goal of leveraging PDE9 inhibition to address unmet needs for patients,” said Howard Surks, MD, Chief Medical and Scientific Officer of Cardurion. “It is gratifying for us to implement this large, global clinical program in partnership with the cardiovascular treatment community. We look forward to receiving the Phase 2 results from these clinical trials and presenting them at a future medical meeting.” Phosphodiesterase (PDE) 9 is an enzyme whose elevated activity in patients with heart failure reduces the beneficial effects of the natriuretic peptide signaling (NPS) pathway. The NPS pathway plays an important and protective role in cardiac function and its activation has been shown to confer outcomes benefit for patients with heart failure. PDE9 is significantly upregulated in patients with chronic heart failure, causing disruption in the NPS pathway. Cardurion is the first company to demonstrate clinical proof-of-mechanism for PDE9 inhibition in patients with chronic heart failure with its PDE9 program. Heart failure is a prevalent and growing condition that is responsible for substantial morbidity and mortality. Approximately 6.7 million adults in the United States suffer from heart failure, and approximately 50 percent of these patients die from the condition within five years of diagnosis. One in five patients with heart failure are hospitalized annually, and approximately 25 percent of these patients are re-admitted within a month of discharge. Approximately half of all patients with chronic heart failure have reduced ejection fraction (HFrEF) and half have preserved ejection fraction (HFpEF), categorized as different diseases based on the pumping ability of the heart. Unmet medical needs remain in heart failure, despite the reductions in morbidity and mortality from currently approved treatments for heart failure. Cardurion Pharmaceuticals is a clinical-stage biotechnology company discovering and developing new therapeutic approaches to address cardiovascular diseases. Cardurion has extensive expertise in cardiovascular biology, signaling pathways and drug discovery and development, and it translates that expertise into potentially groundbreaking therapeutics with the promise to address the unmet needs of patients. Cardurion’s clinical-stage pipeline consists of product candidates targeting phosphodiesterase-9 (PDE9) and calcium/calmodulin-dependent protein kinase II (CaMKII). Cardurion is the first company to advance product candidates against these novel and important targets into clinical testing for the treatment of cardiovascular disease. Cardurion is headquartered in Burlington, Massachusetts, with discovery sciences and research facilities in Shonan, Japan. The content above comes from the network. if any infringement, please contact us to modify.

临床研究

2024-07-17

·Pharmaceutical Technology

Cardurion closes $260m in Series B to develop cardiovascular pipeline

Cardurion also plans to use the funding to expand the indications outlined for the two candidates and acquire additional assets for treating cardiovascular disorders. Image Credit: VectorMine / Shutterstock. US-based cardiology biotech Cardurion Pharmaceuticals has raised $260m in Series B financing to advance its drug pipeline. The proceeds will fund the late-stage trials for two of the company’s lead candidates, CRD-750, a phosphodiesterase 9 (PDE9) inhibitor for heart failure; and CRD-4730, a calmodulin-dependent protein kinase II (CaMKII) inhibitor for treating catecholaminergic polymorphic ventricular tachycardia. Both therapies are being evaluated in Phase II trials. The company also plans to use the fund to expand the number of indications being explored for the two candidates and acquire additional assets for treating cardiovascular disorders. The investors in the Series B round included Bain Capital, Ascenta Capital, and other US-based investment companies. CRD-750 is being evaluated in two Phase II trials (NCT06215586 and NCT06215911) to treat two types of heart failure – heart failure with preserved ejection fraction (HFpEF) and reduced ejection fraction (HFrEF). Both placebo-controlled trials are currently recruiting patients across multiple locations in the US and Canada. In May, the company presented positive data for another PDE9 inhibitor, CRD-740, in patients with heart failure. The CARDINAL-HF Phase IIa trial (NCT05409183) met its primary endpoint in patients with HFrEF by demonstrating a statistically significant median increase in plasma cyclic guanosine monophosphate (cGMP). See Also: Sumitomo Pharma’s DSP-5336 gains FDA fast track for AML AstraZeneca completes Amolyt Pharma acquisition CRD-4730 is being evaluated in a Phase II trial (NCT06005428) as a treatment for catecholaminergic polymorphic ventricular tachycardia—a rare genetic arrhythmic disease. The company also plans to develop CaMKII inhibitors to target additional cardiovascular indications. There has been an increased interest in developing novel cardiovascular therapies in recent months. In February, Novo Nordisk agreed to pay up to $1.46bn to license multiple molecular glue degraders for treating cardiometabolic disorders and rare diseases from Neomorph. As part of the agreement, Neomorph would bear discovery and preclinical research responsibilities while Novo Nordisk would have exclusive rights to further clinical development and commercialisation. Another approach that has emerged as a promising treatment in the cardiovascular space is drugs targeting the glucagon-like peptide-1 (GLP-1) receptor. Last year, Novo Nordisk reported that its GLP-1 therapy Wegovy (semaglutide) reduced the incidence of cardiovascular events in obese and overweight patients by 20% compared to placebo.

临床2期临床结果引进/卖出

2024-07-16

·FierceBiotech

Cardio-focused Cardurion closes hearty $260M series B to challenge statin-dominated status quo

“People see cardio as not just the province of Big Pharma anymore,” Cardurion CEO Peter Lawrence told Fierce Biotech in an interview. Cardurion Pharmaceuticals was made flush in 2021 thanks to a $300 million investment from Bain Capital. Now, the biotech is looking to challenge the statin-dominated cardiovascular status quo with a $260 million series B fundraising round. Bain also participated in this latest raise, which was led by Ascenta Capital. Other new investors include NEA, GV, Fidelity Management & Research Company, Millennium Management, Farallon Capital Management, Invus, Blue Owl Healthcare Opportunities, Delos Capital and Digitalis Ventures. Cardurion was founded by Michael Mendelsohn, M.D., a physician-scientist and previous global head of cardiovascular research at Merck, to develop new therapies for heart failure and other cardiovascular diseases. After forming a collaboration with Takeda in 2017, the biotech emerged with lab space, development resources and licenses to a bunch of Takeda assets. CEO Peter Lawrence, who joined in 2020, credits Cardurion’s success over subsequent years despite a tough market to general excitement about cardiovascular diseases and specific enthusiasm for Cardurion’s first-in-class drugs. “People see cardio as not just the province of Big Pharma anymore,” Lawrence told Fierce Biotech in an interview. “We have two clinical stage assets, three ongoing proof of concept trials, any one of which, if successful, could be somewhat transformational for a patient population.” Cardurion plans to harness the fresh funds to support later-stage clinical trials of its two leading drug candidates, a phosphodiesterase-9 (PDE9) inhibitor called CRD-750 and a calcium–calmodulin-dependent protein kinase II (CaMKII) inhibitor called CRD-4730, both of which are currently in phase 2 clinical trials. CRD-750 is being tested for both types of heart failure: heart failure with preserved ejection fraction, and heart failure with reduced ejection fraction. More than six million adults in the U.S. have heart failure, and heart disease is the leading cause of death in the nation. When the heart is stressed, it depends on a messenger molecule called cyclic guanosine monophosphate (cGMP) to regulate its response. PDE9 plays a role by breaking down cGMP so it isn’t overabundant, but in heart failure, this can lead to a lack of the needed cGMP for the heart to respond to stress. CRD-750 binds to PDE9 and prevents it from breaking down cGMP, which Cardurion thinks will allow the signaling molecule to build up and alleviate heart failure symptoms. “At each step of the way, preclinically and then clinically, the hypothesis has held,” Lawrence said. He believes CRD-750 has the potential to become the standard of care for heart failure. CRD-4730 is being tested for a rare genetic disease called catecholaminergic polymorphic ventricular tachycardia, which causes heart arrhythmia. Cardurion also plans to expand its CaMKII inhibitors into other, more common cardiovascular diseases. “Big Pharma has been trying to get CaMKII inhibitors in the clinic for almost two decades,” Lawrence said. “This is actually the first-ever CaMKII inhibitor that's been taken into human clinical testing.” In addition to furthering its own drugs, Cardurion plans to use series B funds to pursue and purchase other assets. The biotech is currently eyeing one or two preclinical targets that have shown great potential, Lawrence said, and he thinks Cardurion’s robust M&A strategy helped make the company enticing to investors. “It's a high bar because we have great internal assets,” the CEO said. “But if we see something that we love, targets that we think are going to be important, we're going to try and figure out a way to bring them in and get going on them.” Lawrence has been on the other side of the dealmaking table, too; he oversaw the $2.7 billion sale of oncology biotech ArQule to Merck & Co. in 2020. While Cardurion is interested in partnering with Big Pharma, he said, his focus is on pumping up the biotech’s independence. “Having been in and around M&A for 30 years, I think you can never build to [acquisition],” Lawrence said. “We're building the company to have a long gestation.”

临床2期AHA会议

100 项与 Tovinontrine 相关的药物交易

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外链

KEGG	Wiki	ATC	Drug Bank
-	-	-	DB16193

研发状态

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适应症	最高研发状态	国家/地区	公司	日期
慢性心力衰竭	临床2期	美国	Cardurion Pharmaceuticals, Inc.	2024-02-13
慢性心力衰竭	临床2期	澳大利亚	Cardurion Pharmaceuticals, Inc.	2024-02-13
慢性心力衰竭	临床2期	比利时	Cardurion Pharmaceuticals, Inc.	2024-02-13
慢性心力衰竭	临床2期	保加利亚	Cardurion Pharmaceuticals, Inc.	2024-02-13
慢性心力衰竭	临床2期	加拿大	Cardurion Pharmaceuticals, Inc.	2024-02-13
慢性心力衰竭	临床2期	捷克	Cardurion Pharmaceuticals, Inc.	2024-02-13
慢性心力衰竭	临床2期	德国	Cardurion Pharmaceuticals, Inc.	2024-02-13
慢性心力衰竭	临床2期	匈牙利	Cardurion Pharmaceuticals, Inc.	2024-02-13
慢性心力衰竭	临床2期	意大利	Cardurion Pharmaceuticals, Inc.	2024-02-13
慢性心力衰竭	临床2期	拉脱维亚	Cardurion Pharmaceuticals, Inc.	2024-02-13

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研究	分期	人群特征	评价人数	分组	结果	评价	发布日期


NCT04474314 (CTgov)	临床2期	镰状细胞血症	115	IMR-687 (Higher Dose IMR-687)	鬱觸顧襯壓窪繭壓選襯(製醖鏇襯鏇憲鹽艱憲網) = 範憲鹹壓蓋範鬱選網膚簾繭積蓋鏇襯網網醖壓 (壓鬱艱膚壓繭積衊製積, 構積選選夢膚齋壓夢淵 ~ 壓觸鹽蓋醖繭窪膚鹹餘) 更多	-	2023-10-18
				IMR-687 (Lower Dose IMR-687)	鬱觸顧襯壓窪繭壓選襯(製醖鏇襯鏇憲鹽艱憲網) = 範鑰蓋選築鑰醖遞範願簾繭積蓋鏇襯網網醖壓 (壓鬱艱膚壓繭積衊製積, 鏇範簾齋廠糧窪獵簾襯 ~ 遞襯鬱糧蓋壓觸鹽鏇選) 更多
NCT03401112 (IMR-SCD-102, CTgov)	临床2期	镰状细胞血症	100	IMR-687 (IMR-687 50 mg/100 mg)	網繭選鬱鹽鏇獵醖構艱(鏇範網壓糧鹹範網構糧) = 願膚廠鬱艱鑰積蓋顧糧衊膚觸廠襯鹹積繭夢構 (繭糧鑰鹹觸簾醖選築醖, 壓繭顧醖繭獵鹽窪衊鬱 ~ 製鹽蓋窪窪鏇糧齋鹽艱)	-	2022-04-14
				IMR-687 (IMR-687 100 mg/200 mg)	網繭選鬱鹽鏇獵醖構艱(鏇範網壓糧鹹範網構糧) = 憲壓範積淵獵鑰構鬱鏇衊膚觸廠襯鹹積繭夢構 (繭糧鑰鹹觸簾醖選築醖, 鏇遞襯製鑰鑰齋窪遞窪 ~ 壓餘築壓鹹夢蓋遞鏇鏇)
NCT04053803 (ASH 12021 \| ASH 22021) 人工标引	临床2期	镰状细胞血症	24	IMR-687	獵築餘築醖壓願憲繭簾(餘製餘鑰淵選觸憲廠憲) = the most common (≥10%) AEs were headache (21% of subjects), back pain (17%) and nausea (13%) 憲壓構鑰築齋築淵遞膚 (鹹糧齋範鏇壓醖範蓋蓋 ) 更多	积极	2021-11-05
EHA2021	临床2期	镰状细胞血症	93	IMR-687 monotherapy	憲艱顧製齋網壓鏇艱顧(廠製膚鑰衊衊糧廠築淵) = 鏇願鏇鹹顧廠築繭選簾遞醖範獵窪願鏇網糧窪 (醖淵鏇鏇製艱鹽製願顧 )	-	2021-06-09
				IMR-687 + hydroxyurea	憲艱顧製齋網壓鏇艱顧(廠製膚鑰衊衊糧廠築淵) = 夢鹽鹹蓋憲製憲襯獵鬱遞醖範獵窪願鏇網糧窪 (醖淵鏇鏇製艱鹽製願顧 )
NCT03401112 (IMR-SCD-102, EHA2020)	临床2期	镰状细胞血症	57	IMR-687	願膚齋膚襯糧製艱繭鏇(蓋選網窪醖積鬱鹹襯淵) = No AEs leading to discontinuations were noted 觸觸繭獵襯獵窪鹹選憲 (壓顧鬱築壓觸鹽鑰糧願 ) 更多	积极	2020-05-14