VEGFR2 peptide vaccine(Merck Serono SA)(VEGFR2 peptide vaccine(Merck Serono SA)) - 药物靶点：VEGFR2_在研适应症：胶质瘤，复发性胶质母细胞瘤，结直肠癌_专利_临床

概要

基本信息

药物类型

通用抗原疫苗、合成肽疫苗、治疗性疫苗

别名

VEGFR2 peptide vaccine、VEGFR2 specific T cell vaccine、VXM 01

+ [1]

靶点

VEGFR2

作用机制

VEGFR2拮抗剂(血管内皮细胞生长因子受体2拮抗剂)

治疗领域

肿瘤神经系统疾病其他疾病+ [2]

在研适应症

胶质瘤复发性胶质母细胞瘤结直肠癌+ [1]

非在研适应症

结肠癌肝转移转移性结直肠癌胰腺继发性恶性肿瘤

原研机构

Merck Serono SA

在研机构

Merck Serono SAMerck KGaA

Vaximm AG

非在研机构

康哲药业

最高研发阶段临床2期

首次获批日期-

最高研发阶段(中国)无进展

特殊审评-

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序列信息

Sequence Code 117962

靶点: *****

关联

4

项与 VEGFR2 peptide vaccine(Merck Serono SA) 相关的临床试验

NCT03750071 / Active, not recruiting临床1/2期

An Open-label, Phase I/II Multicenter Clinical Trial of VXM01 in Combination With Avelumab in Patients With Progressive Glioblastoma Following Standard Treatment, With or Without Second Surgery

VXM01 in combination with avelumab in n=30 patients with progressive glioblastoma following standard treatment, with or without second surgery

开始日期2018-11-21

申办/合作机构

Vaximm AG

[+2]

NCT02718443 / Completed临床1期

VXM01 Phase I Pilot Study in Patients With Operable Recurrence of a Glioblastoma to Examine Safety, Tolerability, Immune and Biomarker Response to the Investigational VEGFR-2 DNA Vaccine VXM01

VXM01 phase I pilot study in patients with operable recurrence of a glioblastoma to examine safety, tolerability, immune and biomarker response to the investigational VEGFR-2 DNA vaccine VXM01

开始日期2016-05-01

申办/合作机构

Vaximm AG

NCT02718430 / Completed临床1期

VXM01 Phase I Study in Patients With Metastatic Colorectal Cancer With Liver Metastasis Under Second or Third Line Therapy to Examine Safety, Efficacy, and Immune Biomarkers After Treatment With VXM01

Phase I study in patients with metastatic colorectal cancer with liver metastasis under second or third line therapy to examine safety, efficacy, and immune biomarkers after treatment with VXM01

开始日期2016-02-01

申办/合作机构

Vaximm AG

100 项与 VEGFR2 peptide vaccine(Merck Serono SA) 相关的临床结果

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100 项与 VEGFR2 peptide vaccine(Merck Serono SA) 相关的转化医学

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100 项与 VEGFR2 peptide vaccine(Merck Serono SA) 相关的专利（医药）

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123

项与 VEGFR2 peptide vaccine(Merck Serono SA) 相关的文献（医药）

2024-05-31·BMB reports

MMPP is a novel VEGFR2 inhibitor that suppresses angiogenesis via VEGFR2/AKT/ERK/NF-κB pathway

作者: Lee, Hee Pom ; Park, Jae-Young ; Shin, Ha Youn ; Yoon, Do-Young ; Kim, Na-Yeon ; Park, Hyo-Min ; Kim, Uijin ; Hong, Jin Tae

Many types of cancer are associated with excessive angiogenesis. Anti-angiogenic treatment is an effective strategy for treating solid cancers. This study aimed to demonstrate the inhibitory effects of (E)-2-methoxy-4-(3-(4-methoxyphenyl) prop-1-en-1-yl) phenol (MMPP) in VEGFA-induced angiogenesis. The results indicated that MMPP effectively suppressed various angiogenic processes, such as cell migration, invasion, tube formation, and sprouting of new vessels in human umbilical vein endothelial cells (HUVECs) and mouse aortic ring. The inhibitory mechanism of MMPP on angiogenesis involves targeting VEGFR2. MMPP showed high binding affinity for the VEGFR2 ATP-binding domain. Additionally, MMPP improved VEGFR2 thermal stability and inhibited VEGFR2 kinase activity, suppressing the downstream VEGFR2/AKT/ERK pathway. MMPP attenuated the activation and nuclear translocation of NF-κB, and it downregulated NF-κB target genes such as VEGFA, VEGFR2, MMP2, and MMP9. Furthermore, conditioned medium from MMPP-treated breast cancer cells effectively inhibited angiogenesis in endothelial cells. These results suggested that MMPP had great promise as a novel VEGFR2 inhibitor with potent anti-angiogenic properties for cancer treatment via VEGFR2/AKT/ERK/NF-κB signaling pathway. [BMB Reports 2024; 57(5): 244-249].

2024-04-01·Heliyon

Evaluation of the efficacy and safety of ramucirumab combined with nab-paclitaxel, lobaplatin, and S-1 in neoadjuvant and conversion therapy for advanced gastric cancer: A study protocol of prospective single-center, randomized controlled and open label clinical trial (RNPLS-01)

Article

作者: Wang, Juan ; Li, Mengbin ; Zhao, Yan ; Liu, Shushang ; Wang, Shu ; Wang, Yuhao ; Ma, Yuxuan ; Ji, Gang ; Yang, Jianjun ; Huo, Huade ; Wang, Haoyuan ; Xu, Guanghui ; Peng, Chaosheng ; Li, Haolin

Objective:

Ramucirumab is a VEGFR2 antagonist. The aim of this trial is to evaluate the efficacy and safety of ramucirumab combined with nab-paclitaxel, lobaplatin and S-1 in neoadjuvant and conversion therapy for advanced gastric cancer.

Methods:

and analysis: This study is a prospective single-center, randomized controlled and open label clinical study, enrolling a total of 140 patients with advanced gastric cancer distributed across two distinct cohorts (Cohort A n = 70; Cohort B n = 70). The central focus of the study lies in evaluating the pathological complete response (pCR) of the cancer post-neoadjuvant or conversion therapy. Secondary endpoints encompass the assessment of the R0 resection rate subsequent to the aforementioned therapies, the occurrence of adverse events (AE), progression-free survival (PFS), overall survival (OS), the objective response rate (ORR), the total response rate and its duration, the disease control rate (DCR), and the duration of overall response (DOR).

Ethics:

Ethics approval has been obtained from the Ethics Committee at the First Affiliated Hospital (Xijing Hospital) of Air force Military Medical University (KY20232220-F-1).

Trial registration:

This trial has been registered at the ClinicalTrials.gov: NCT06169410 (registration date: December 5, 2023).

2024-04-01·International immunopharmacology

CPD-002, a novel VEGFR2 inhibitor, relieves rheumatoid arthritis by reducing angiogenesis through the suppression of the VEGFR2/PI3K/AKT signaling pathway

Article

作者: Li, Fei-Long ; Jiang, Fei ; Zhang, Man-Yu ; Liu, Xue-Song ; Xie, Ya-Wen ; Huang, Yan ; Zhang, Pei-Pei ; Yang, Yu-Chen ; Zhou, Meng-Yuan ; Li, Rong ; Gu, Sheng-Long ; Wang, Meng-Qing

Synovial angiogenesis is a key player in the development of rheumatoid arthritis (RA), and anti-angiogenic therapy is considered a promising approach for treating RA. CPD-002 has demonstrated efficacy in suppressing tumor angiogenesis as a VEGFR2 inhibitor, but its specific impacts on RA synovial angiogenesis and possible anti-RA effects need further study. We examined the influences of CPD-002 on the migration and invasion of human umbilical vein endothelial cells (HUVECs) and its impacts on HUVECs' tube formation and vessel sprouting ex vivo. The therapeutic potential of CPD-002 in adjuvant-induced arthritis (AIA) rats and its suppression of synovial angiogenesis were examined. The involvement of the VEGFR2/PI3K/AKT pathway was assessed both in HUVECs and AIA rat synovium. Here, CPD-002 inhibited the migration and invasion of VEGF-stimulated HUVECs, decreased their chemotactic response to RA fibroblast-like synoviocyte-released chemoattractants, and exhibited anti-angiogenic effects in vitro and ex vivo. CPD-002's targeting of VEGFR2 was confirmed with molecular docking and cellular thermal shift assays, supported by the abolishment of CPD-002's effects upon using VEGFR2 siRNA. CPD-002 relieved paw swelling, arthritis index, joint damage, and synovial angiogenesis, indicating its anti-arthritic and anti-angiogenic effects in AIA rats. Moreover, the anti-inflammatory effects in vivo and in vitro of CPD-002 contributed to its anti-angiogenic effects. Mechanistically, CPD-002 hindered the activation of VEGFR2/PI3K/AKT pathway in VEGF-induced HUVECs and AIA rat synovium, as evidenced by reduced p-VEGFR2, p-PI3K, and p-AKT protein levels alongside elevated PTEN protein levels. Totally, CPD-002 showed anti-rheumatoid effects via attenuating angiogenesis through the inhibition of the VEGFR2/PI3K/AKT pathway.

2

项与 VEGFR2 peptide vaccine(Merck Serono SA) 相关的新闻（医药）

2023-07-12

·FierceBiotech

South Korean biotech group spies US SPAC as route to Nasdaq

The plan is to take the holding company onto the Nasdaq under the new name OSR Biosciences in the fourth quarter. OSR Holdings is the latest biotech business to choose a merger with a special purpose acquisition company (SPAC) as a way to hop onto the public markets. Seoul, South Korea-headquartered OSR is a global healthcare holding company with operations including a pair of subsidiaries in South Korea and Switzerland focused on developing drugs for oncology and osteoarthritis. The company also owns a distributor of medical devices for neurovascular and other diseases and last week announced plans to acquire Landmark BioVentures, another Swiss company that operates four oncology- and immunology-focused biotech ventures in France. The latest announcement will see OSR merge with U.S.-based Bellevue Life Sciences Acquisition. The SPAC went public in February with a $60 million IPO and the goal of finding a suitable healthcare-focused company to join forces with. In OSR, it appears to have found the desired target, and the plan is to take the holding company onto the Nasdaq under the new name OSR Biosciences in the fourth quarter of the year. The only clinical-stage candidate in OSR’s portfolio is VXM01, an immunotherapy in phase 1/2 development by the Swiss-German biotech Vaximm for glioblastoma in combination with Merck KGaA’s Bavencio. Vaximm also has therapies targeting the proteins mesothelin, WT1 and PD-L1 in preclinical development. "We are delighted to identify OSR Holdings as our candidate,” Bellevue Life Sciences Acquisition's CEO Kuk Hyoun Hwang said in a postmarket release yesterday. “OSR Holdings represents a timely investment opportunity working on the development of breakthrough therapies for unmet medical needs." While SPAC deals were a hot ticket for biotechs to go public a couple of years ago, the rush cooled in 2022 as the industry hit tough times. Since then, their use has been more sporadic, with some companies testing the SPAC waters again near the year’s end. This spring also saw a trickle of merger announcements, with Anew Medical, enGene and NKGen Biotech all opting for the blank check route to market.

并购IPO

2012-10-02

·BioSpace

VAXIMM Receives Grant to Expand Pipeline of Oral Cancer Vaccines

Basel (Switzerland), Mannheim (Germany), October 2nd, 2012 – VAXIMM AG, a Swiss-German biotech company focusing on cancer vaccines, today announced that its German subsidiary VAXIMM GmbH has been awarded a grant from the leading-edge BioRN cluster “Cell-based and Molecular Medicine” to expand its oral T-cell vaccine technology platform. The cluster competition is a program of Germany´s Federal Ministry of Education and Research (BMBF) to promote top-notch innovation in Germany. VAXIMM’s lead candidate VXM01 is an oral T-cell vaccine, which targets the tumor vasculature. It is currently in Phase I/II clinical evaluation in pancreatic cancer patients at the Heidelberg University Hospital. The funding from the leading-edge cluster program will be used to develop additional cancer vaccines complementary to VXM01, which are based on the same oral T-cell vaccine technology. A second candidate (VXM06), which targets an undisclosed, abundant, tumor-specific antigen, is already in preclinical development. Two further product candidates are at discovery stage. VAXIMM’s oral T-cell vaccine technology has a number of advantages. The platform can easily and rapidly generate new vaccines, including multivalent vaccines. The resulting products combine oral efficacy with safety and excellent tolerability. Moreover, the vaccines do not require a complex manufacturing infrastructure. “We are pleased about the recognition of the potential of our oral T-cell vaccination platform,” said Dr. Heinz Lubenau, General Manager of VAXIMM GmbH. “It allows leveraging our work on VXM01 to add additional products to our promising pipeline.” About VAXIMMs Oral T-cell Vaccine Technology: VAXIMM's oral T-cell vaccine platform is based on an approved, live attenuated bacterial vaccine strain, which has been applied in millions of individuals for prophylactic vaccination, and is safe and well tolerated. To yield its oral T-cell vaccines, this strain is modified to carry the genetic information of a specific target antigen. After oral vaccination with such modified bacteria, patients are mounting a strong specific cellular immune response against the target. So-called killer cells of the immune system are then targeting and destroying the corresponding cancer or cancer-associated cells. As a result, the tumor shrinks, while metastasis formation and growth are inhibited. The scalable platform offers many advantages, such as oral efficacy, good tolerability, and ease and low cost of candidate generation and manufacturing. About VAXIMM: VAXIMM is a privately held, Swiss- and German-based biotech company that is primarily focused on developing active immunotherapies (vaccines) for patients suffering from cancer. Its initial product candidate VXM01 is targeting the tumor vasculature, which is essential for tumors to grow beyond microscopic size. VXM01 has shown impressive anti-tumor activity in numerous animal studies and commenced human clinical trials in 2011. VAXIMM was formed in 2008 as a joint venture of BB Biotech Ventures and Merck KGaA to develop VXM01. Merck Serono Ventures, Sunstone Capital, and BioMedPartners joined as investors in 2010. VAXIMM GmbH is a fully owned subsidiary of VAXIMM AG, located in Mannheim, Germany. For more information, please see Contact: Dr. Heinz Lubenau Tel.: +49 621 8359 687 10 Email: info@vaximm.com Media Inquiries: akampion Dr. Ludger Wess / Ines-Regina Buth Managing Partners info@akampion.com Tel. +49 40 88 16 59 64 Tel. +49 30 23 63 27 68

疫苗

100 项与 VEGFR2 peptide vaccine(Merck Serono SA) 相关的药物交易

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研发状态

10 条进展最快的记录,

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适应症	最高研发状态	国家/地区	公司	日期
胶质母细胞瘤	临床2期	法国	Vaximm AG	2018-11-21
胶质母细胞瘤	临床2期	德国	Vaximm AG	2018-11-21
胶质母细胞瘤	临床2期	荷兰	Vaximm AG	2018-11-21
复发性胶质母细胞瘤	临床2期	德国	Merck KGaA	2018-11-21
复发性胶质母细胞瘤	临床2期	德国	Vaximm AG	2018-11-21
胶质瘤	临床2期	-	Merck Serono SA	-
结肠癌肝转移	临床1期	德国	Vaximm AG	2016-02-01
转移性结直肠癌	临床1期	德国	Vaximm AG	2016-02-01
胰腺继发性恶性肿瘤	临床1期	德国	Vaximm AG	2011-12-01
结直肠癌	临床1期	-	Merck Serono SA	-

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临床结果

适应症

分期

评价

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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


NCT03750071 (ASCO2020) 人工标引	临床1/2期	胶质母细胞瘤	30	avelumab+VXM01	醖襯餘廠淵鹹鹽衊衊衊(襯簾鬱鏇鏇餘衊顧獵選) = 繭鹹鏇繭構遞襯憲憲壓觸簾壓襯製夢繭網觸糧 (鏇醖蓋顧窪遞窪糧膚憲 ) 更多	积极	2020-05-29
AACR2019	N/A	-	-	Erlotinib+VEGFR-2 inhibitor	廠糧選鏇蓋艱衊築範餘(鬱鹹鏇鬱醖顧膚築膚鑰) = 淵淵襯憲製襯鏇襯夢選膚構繭製獵築衊齋選憲 (衊襯遞蓋顧積觸築簾衊 )	-	2019-07-01
AACR2019	N/A	-	-	Erlotinib alone	廠糧選鏇蓋艱衊築範餘(鬱鹹鏇鬱醖顧膚築膚鑰) = 蓋鏇簾襯醖網膚製選獵膚構繭製獵築衊齋選憲 (衊襯遞蓋顧積觸築簾衊 )	-	2019-07-01
ESMO2018	N/A	继发性肺恶性肿瘤	44	Apatinib	襯顧觸醖獵膚選築願獵(構鬱選鑰衊觸簾蓋範獵) = AEs greater than degree 2 was seen in 50.0%, including pneumothorax in 11 cases (25.0%) 壓鑰願膚衊鏇齋鏇築築 (顧構醖積憲齋觸繭獵築 ) 更多	积极	2018-10-22
NCT02718443 (ASCO2018) 人工标引	临床1期	胶质母细胞瘤	14	VEGFR2 peptide vaccine	鑰鑰憲壓膚鏇鹹遞範鑰(鏇糧遞艱鹹鑰鏇鏇膚糧) = 膚製積積範壓膚顧範鑰積艱醖衊築壓選願蓋淵 (簾選鹽顧繭膚襯壓構觸 ) 更多	积极	2018-06-02
ASCO2016	临床1期	胰腺癌	-	VXM01	繭夢鹹鹽膚顧觸壓築艱(糧鏇窪蓋製廠淵積餘顧) = Drug-related adverse events preferentially associated with boosting doses of VXM01 were decreases in lymphocyte count (22% vs 0) 淵鏇醖餘鹹構網鏇窪壓 (製範餘醖蓋選鏇獵網襯 ) 更多	积极	2016-05-20
ASCO2016	临床1期	胰腺癌	-	Placebo		积极	2016-05-20
ASCO2009	临床1期	胰腺癌	18	VEGFR2-epitope peptide	膚齋築壓網遞餘淵壓網(憲積築糧鹹淵膚積襯淵) = 鹽淵觸簾獵鹹鑰簾蓋遞遞願蓋願簾蓋鹽膚顧鹹 (襯鑰遞襯願齋鹹鬱製繭 ) 更多	-	2009-05-20