View ValuationThis company listing is no longer activeThis company may still be operating, however this listing is no longer active. Find out why through their latest events.See Latest EventsVivesto 향후 성장Future 기준 점검 0/6Vivesto 의 수익이 23%로 연간 감소할 전망입니다. 주당 순이익은 감소 연간 0.01%만큼 감소할 것으로 예상됩니다.핵심 정보-23.0%이익 성장률-0.0066%EPS 성장률Biotechs 이익 성장25.3%매출 성장률n/a향후 자기자본이익률-50.40%애널리스트 커버리지Low마지막 업데이트02 Mar 2026최근 향후 성장 업데이트업데이트 없음모든 업데이트 보기Recent updates공시 • Jan 24Vivesto AB has completed a Follow-on Equity Offering in the amount of SEK 53.804346 million.Vivesto AB has completed a Follow-on Equity Offering in the amount of SEK 53.804346 million. Security Name: Shares Security Type: Common Stock Securities Offered: 538,043,455 Price\Range: SEK 0.1 Transaction Features: Rights Offering공시 • Nov 20Vivesto AB has filed a Follow-on Equity Offering in the amount of SEK 53.804346 million.Vivesto AB has filed a Follow-on Equity Offering in the amount of SEK 53.804346 million. Security Name: Shares Security Type: Common Stock Securities Offered: 538,043,455 Price\Range: SEK 0.1 Transaction Features: Rights Offering공시 • Nov 08Vivesto AB, Annual General Meeting, May 07, 2026Vivesto AB, Annual General Meeting, May 07, 2026. Location: stockholm Sweden공시 • Apr 08Vivesto AB, Annual General Meeting, May 08, 2025Vivesto AB, Annual General Meeting, May 08, 2025, at 09:00 W. Europe Standard Time. Location: at gustav iii:s boulevard 42, ground floor, se-169 73 solna, Sweden공시 • Apr 01Vivesto AB Reports Positive Cantrixil Results in an Animal Hematological Cancer ModelVivesto AB announced that positive preclinical efficacy data was obtained in an animal model of hematological cancer. The results support continued development of the candidate drug Cantrixil within this indication and are in line with previous positive preclinical data. The experimental trial demonstrates, for the first time, that Cantrixil can reduce tumor growth and increase survival times in a well-established mouse model of hematological cancer. The treatment was well tolerated and safe. With the new positive data, Vivesto is continuing the planning of activities needed to bring Cantrixil into clinical trials and in parallel will investigate opportunities to partner the project in order to optimize the development program.공시 • Jan 16Vivesto AB Receives Approval to Initiate A Dose-Finding Study of Paccal Vet in CatsVivesto AB announced that ethical approval has been obtained from the US Veterinary Review Board Clinical Studies Committee for a planned Paccal Vet dose-finding clinical trial in cats with cancer. The approval authorizes the participating clinical sites to enroll patients in the study. The dose-finding study will initially be conducted at two clinical sites in Washington and Oregon, with the possibility to include more sites as the study progresses. The study will be managed by CASTR Alliance, the contract research organization (CRO) currently running Paccal Vet's pilot clinical trial in dogs with splenic hemangiosarcoma in the US. FDA's Center for Veterinary Medicine, CVM, has previously confirmed that the cat study can be conducted under the existing INAD (Investigational New Animal Drug). The dose-finding study will follow the 3+3 design, a widely used approach to determine the maximum tolerated dose (MTD). A maximum of 12 cats will be included, receiving Paccal Vet treatment in groups of three, with doses escalating for each group until the MTD is identified. This study design ensures patient safety while effectively identifying the appropriate dosage for Paccal Vet administration in cats.공시 • Dec 20Vivesto Strengthens Cantrixil Program with New Preclinical Results and Patent ApplicationVivesto AB, announced that positive results were obtained from preclinical studies with combination treatments within the company’s Cantrixil program, supporting continued development in hematological cancer. Vivesto also announced that a new patent application covering the treatment of hematological cancer with Cantrixil was filed, with the aim to strengthen the IP position. The drug candidate Cantrixil has been evaluated in further combination treatments with other anti-cancer drugs generating new in vitro data in hematological cancer cell lines. The results demonstrate clear positive effects of Cantrixil in combination with other anti-cancer drugs. The positive results confirm previous preclinical efficacy results and support continued development in hematological cancer. New results from hematological cancer models are expected to be presented throughout 2025. Cantrixil has previously shown strong cytotoxic effects at low doses in cell lines derived from patients with hematological cancer. The recently generated data provides important input to the dosing selection and treatment regime in upcoming preclinical and clinical studies.공시 • Jan 30Vivesto's International Patent Application for XR-18 Receives Positive DecisionVivesto AB, announced that the European Patent Office (EPO) has granted a positive approval regarding the patentability of the company's XR-18 technology platform in Vivesto's international patent application (Patent Cooperation Treaty; PCT). The patent application for XR-18 is now in an international phase, which provides the opportunity to apply for patents in countries that are part of the PCT collaboration (157 countries). Vivesto now has two independent assessments that have been positive about the patentability of the XR-18 invention; EPO and earlier from the Swedish Intellectual Property Office (PRV). The company will now evaluate in which countries the company intends to seek protection.공시 • Dec 28Vivesto AB's US Clinical Paccal Vet Trial Receives Approval to Start Patient RecruitmentVivesto AB announced that the US Veterinary Review Board Clinical Studies Committee approved the company's planned Paccal Vet open label, pilot clinical study in dogs with splenic hemangiosarcoma following splenectomy. Clinical sites have been chosen and will be ready to start activities after supply of Paccal Vet (investigational veterinary product, IVP) in January. A planned interim analysis is expected in the second half of 2024. The Paccal Vet development program was discussed with FDA earlier this year. No further Agency approval is required prior to study start. The study is an open label, exploratory indication finding study in dogs with different stages of splenic hemangiosarcoma (HSA) following splenectomy. The study will include 4 treatment cycles of Paccal Vet (paclitaxel micellar) and it is planned to investigate 2 cohorts. Each cohort is planned to include a maximum of 23 patients. The study will be conducted at 6 clinical sites in Washington and Oregon. First patients are expected to be dosed in early 2024 and a planned interim analysis is expected in the second half of 2024. If promising activity in either cohort is shown, the study shall be followed by a pivotal study designed to confirm the initial findings of this pilot study and to gather further evidence on the safety and efficacy of Paccal Vet in dogs with splenic hemangiosarcoma. Vivesto's drug candidate Paccal Vet consists of paclitaxel formulated with the company's proprietary XR-17 technology. Vivesto has previously shown good safety of Paccal Vet in the treatment of various types of cancer in dogs. The absence of the solvent cremophor, to which dogs are particularly sensitive, may reduce the risk of serious side effects and death associated to the treatment. Paccal Vet also does not require the addition of human albumin, which when used in dogs can cause hypersensitivity reactions and reduced treatment effectiveness.공시 • Nov 24Vivesto AB (publ) Announces Composition of Nomination CommitteeIn accordance with the principles for appointing a Nomination Committee, which were adopted at Vivesto AB's Annual General Meeting in 2022, it is hereby announced that the Nomination Committee for the 2024 Annual General Meeting has been appointed, based on the ownership structure as per 30 September 2023. The Nomination Committee for the 2024 Annual General Meeting comprises the following members: Per Arwidsson, appointed by Arwidsro, Håkan Lagerberg, appointed by Mastan AB, and Peter Zonabend, Chairman of the Board of Vivesto. Per Arwidsson has been appointed Chairman of the Nomination Committee.공시 • Nov 18Vivesto AB, Annual General Meeting, May 23, 2024Vivesto AB, Annual General Meeting, May 23, 2024.공시 • Nov 17+ 2 more updatesVivesto AB to Report Nine Months, 2024 Results on Nov 21, 2024Vivesto AB announced that they will report nine months, 2024 results on Nov 21, 2024공시 • Aug 05Vivesto AB Announces Early Termination of Patient Enrollment in the Investigator-Initiated Phase 1B Docetaxel Micellar StudyVivesto AB announced early termination of patient enrollment in the Docetaxel micellar advanced prostate cancer Phase 1b study with the Swiss Group for Clinical Cancer Research (SAKK). The open-label, multicenter, single-stage Phase 1b study has closed its accrual after enrollment of 11 of the planned 18 patients, since Vivesto believes that the data generated will be sufficient ahead of switching into development with a new formulation based on its improved XR-18 micelle technology platform. Docetaxel mousellar has shown good tolerability at doses considered standard for conventional docetaxel formulations, as well as signs of clinical activity. Docetaxel miceLLar has been well received by investigators of the SAKK 67/20 and by participating prostate cancer patients. Vivesto's Docetaxel micellAR is a solvent-free formulation of docetaxel developed to avoid the need for the solubility enhancers in a solvent-based docetaxel and the mandatory high-dose steroid premedication. Patients treated with other existing formulations of docetaxel require steroid administration to avoid certain serious adverse events related to the formulations with solvent. The administration of steroids can lead to marked bone fragility, exacerbated by cancer metastases in the bone, or steroid-related metabolic issues. Vivesto has progressed in the development of its XR-18 drug delivery platform and intends to use this next-generation improved technology in future development of Docetaxel miceller.공시 • Nov 17+ 3 more updatesVivesto AB to Report Fiscal Year 2023 Results on Feb 23, 2024Vivesto AB announced that they will report fiscal year 2023 results on Feb 23, 2024이익 및 매출 성장 예측OTCPK:OASM.Y - 애널리스트 향후 추정치 및 과거 재무 데이터 (SEK Millions)날짜매출이익자유현금흐름영업현금흐름평균 애널리스트 수12/31/2028N/A-62-62-62112/31/2027N/A-48-51-51112/31/2026N/A-31-29-29112/31/2025N/A-34-44-34N/A9/30/2025N/A-36-41-31N/A6/30/2025N/A-39-50-40N/A3/31/2025N/A-40-39-33N/A12/31/2024N/A-40-47-47N/A9/30/20247-93-46-46N/A6/30/20247-99-54-53N/A3/31/20247-117-62-62N/A12/31/20237-129-69-69N/A9/30/20232-284-88-88N/A6/30/20233-340-92-91N/A3/31/20233-351-89-88N/A12/31/20223-357-86-86N/A9/30/202213-140-105-104N/A6/30/202224-99-107-107N/A3/31/202229-118-134-133N/A12/31/202129-133-180-146N/A9/30/2021-184-348-358-324N/A6/30/2021-195-354-378-341N/A3/31/2021-199-376-216-178N/A12/31/20204-210-211-205N/A10/31/2020205-59-19-11N/A7/31/2020205-24-56-47N/A4/30/2020206-11-19-7N/A1/31/20204-196-198-187N/A10/31/20196-167N/A-168N/A7/31/20199-210N/A-134N/A4/30/201910-201N/A-119N/A1/31/201914-154N/A-104N/A10/31/201813-153N/A-97N/A7/31/201813-117N/A-103N/A4/30/201812-118N/A-124N/A1/31/201810-128N/A-124N/A10/31/201710-139N/A-144N/A7/31/20178-155N/A-134N/A4/30/20177-160N/A-133N/A1/31/20177-151N/A-145N/A10/31/201616-137N/A-147N/A7/31/201619-139N/A-142N/A4/30/201623-142N/A-128N/A1/31/201626-139N/A-112N/A10/31/201518-141N/A-93N/A7/31/201519-124N/A-101N/A4/30/201519-117N/A-108N/A더 보기애널리스트 향후 성장 전망수입 대 저축률: OASM.Y 향후 3년 동안 수익성이 없을 것으로 예상됩니다.수익 vs 시장: OASM.Y 향후 3년 동안 수익성이 없을 것으로 예상됩니다.고성장 수익: OASM.Y 향후 3년 동안 수익성이 없을 것으로 예상됩니다.수익 대 시장: OASM.Y 의 수익이 US 시장보다 빠르게 증가할 것으로 예상되는지 판단하기에는 데이터가 부족합니다.고성장 매출: OASM.Y 은(는) 내년에 수익이 없을 것으로 예상됩니다.주당순이익 성장 예측향후 자기자본이익률미래 ROE: OASM.Y는 3년 뒤에도 수익성이 없을 것으로 전망됩니다.성장 기업 찾아보기7D1Y7D1Y7D1YPharmaceuticals-biotech 산업의 고성장 기업.View Past Performance기업 분석 및 재무 데이터 상태데이터최종 업데이트 (UTC 시간)기업 분석2026/04/28 05:49종가2026/02/10 00:00수익2025/12/31연간 수익2025/12/31데이터 소스당사의 기업 분석에 사용되는 데이터는 S&P Global Market Intelligence LLC에서 제공됩니다. 아래 데이터는 이 보고서를 생성하기 위해 분석 모델에서 사용됩니다. 데이터는 정규화되므로 소스가 제공된 후 지연이 발생할 수 있습니다.패키지데이터기간미국 소스 예시 *기업 재무제표10년손익계산서현금흐름표대차대조표SEC 양식 10-KSEC 양식 10-Q분석가 컨센서스 추정치+3년재무 예측분석가 목표주가분석가 리서치 보고서Blue Matrix시장 가격30년주가배당, 분할 및 기타 조치ICE 시장 데이터SEC 양식 S-1지분 구조10년주요 주주내부자 거래SEC 양식 4SEC 양식 13D경영진10년리더십 팀이사회SEC 양식 10-KSEC 양식 DEF 14A주요 개발10년회사 공시SEC 양식 8-K* 미국 증권에 대한 예시이며, 비(非)미국 증권에는 해당 국가의 규제 서식 및 자료원을 사용합니다.별도로 명시되지 않는 한 모든 재무 데이터는 연간 기간을 기준으로 하지만 분기별로 업데이트됩니다. 이를 TTM(최근 12개월) 또는 LTM(지난 12개월) 데이터라고 합니다. 자세히 알아보기.분석 모델 및 스노우플레이크이 보고서를 생성하는 데 사용된 분석 모델에 대한 자세한 내용은 당사의 Github 페이지에서 확인하실 수 있습니다. 또한 보고서 활용 방법에 대한 가이드와 YouTube 튜토리얼도 제공합니다.Simply Wall St 분석 모델을 설계하고 구축한 세계적 수준의 팀에 대해 알아보세요.산업 및 섹터 지표산업 및 섹터 지표는 Simply Wall St가 6시간마다 계산하며, 프로세스에 대한 자세한 내용은 Github에서 확인할 수 있습니다.분석가 소스Vivesto AB는 5명의 분석가가 다루고 있습니다. 이 중 1명의 분석가가 우리 보고서에 입력 데이터로 사용되는 매출 또는 수익 추정치를 제출했습니다. 분석가의 제출 자료는 하루 종일 업데이트됩니다.분석가기관Camilla OxhamreCarnegie Investment Bank ABKlas PalinDNB Carnegie Commissioned ResearchSusie JanaEdison Investment Research2명의 분석가 더 보기
공시 • Jan 24Vivesto AB has completed a Follow-on Equity Offering in the amount of SEK 53.804346 million.Vivesto AB has completed a Follow-on Equity Offering in the amount of SEK 53.804346 million. Security Name: Shares Security Type: Common Stock Securities Offered: 538,043,455 Price\Range: SEK 0.1 Transaction Features: Rights Offering
공시 • Nov 20Vivesto AB has filed a Follow-on Equity Offering in the amount of SEK 53.804346 million.Vivesto AB has filed a Follow-on Equity Offering in the amount of SEK 53.804346 million. Security Name: Shares Security Type: Common Stock Securities Offered: 538,043,455 Price\Range: SEK 0.1 Transaction Features: Rights Offering
공시 • Nov 08Vivesto AB, Annual General Meeting, May 07, 2026Vivesto AB, Annual General Meeting, May 07, 2026. Location: stockholm Sweden
공시 • Apr 08Vivesto AB, Annual General Meeting, May 08, 2025Vivesto AB, Annual General Meeting, May 08, 2025, at 09:00 W. Europe Standard Time. Location: at gustav iii:s boulevard 42, ground floor, se-169 73 solna, Sweden
공시 • Apr 01Vivesto AB Reports Positive Cantrixil Results in an Animal Hematological Cancer ModelVivesto AB announced that positive preclinical efficacy data was obtained in an animal model of hematological cancer. The results support continued development of the candidate drug Cantrixil within this indication and are in line with previous positive preclinical data. The experimental trial demonstrates, for the first time, that Cantrixil can reduce tumor growth and increase survival times in a well-established mouse model of hematological cancer. The treatment was well tolerated and safe. With the new positive data, Vivesto is continuing the planning of activities needed to bring Cantrixil into clinical trials and in parallel will investigate opportunities to partner the project in order to optimize the development program.
공시 • Jan 16Vivesto AB Receives Approval to Initiate A Dose-Finding Study of Paccal Vet in CatsVivesto AB announced that ethical approval has been obtained from the US Veterinary Review Board Clinical Studies Committee for a planned Paccal Vet dose-finding clinical trial in cats with cancer. The approval authorizes the participating clinical sites to enroll patients in the study. The dose-finding study will initially be conducted at two clinical sites in Washington and Oregon, with the possibility to include more sites as the study progresses. The study will be managed by CASTR Alliance, the contract research organization (CRO) currently running Paccal Vet's pilot clinical trial in dogs with splenic hemangiosarcoma in the US. FDA's Center for Veterinary Medicine, CVM, has previously confirmed that the cat study can be conducted under the existing INAD (Investigational New Animal Drug). The dose-finding study will follow the 3+3 design, a widely used approach to determine the maximum tolerated dose (MTD). A maximum of 12 cats will be included, receiving Paccal Vet treatment in groups of three, with doses escalating for each group until the MTD is identified. This study design ensures patient safety while effectively identifying the appropriate dosage for Paccal Vet administration in cats.
공시 • Dec 20Vivesto Strengthens Cantrixil Program with New Preclinical Results and Patent ApplicationVivesto AB, announced that positive results were obtained from preclinical studies with combination treatments within the company’s Cantrixil program, supporting continued development in hematological cancer. Vivesto also announced that a new patent application covering the treatment of hematological cancer with Cantrixil was filed, with the aim to strengthen the IP position. The drug candidate Cantrixil has been evaluated in further combination treatments with other anti-cancer drugs generating new in vitro data in hematological cancer cell lines. The results demonstrate clear positive effects of Cantrixil in combination with other anti-cancer drugs. The positive results confirm previous preclinical efficacy results and support continued development in hematological cancer. New results from hematological cancer models are expected to be presented throughout 2025. Cantrixil has previously shown strong cytotoxic effects at low doses in cell lines derived from patients with hematological cancer. The recently generated data provides important input to the dosing selection and treatment regime in upcoming preclinical and clinical studies.
공시 • Jan 30Vivesto's International Patent Application for XR-18 Receives Positive DecisionVivesto AB, announced that the European Patent Office (EPO) has granted a positive approval regarding the patentability of the company's XR-18 technology platform in Vivesto's international patent application (Patent Cooperation Treaty; PCT). The patent application for XR-18 is now in an international phase, which provides the opportunity to apply for patents in countries that are part of the PCT collaboration (157 countries). Vivesto now has two independent assessments that have been positive about the patentability of the XR-18 invention; EPO and earlier from the Swedish Intellectual Property Office (PRV). The company will now evaluate in which countries the company intends to seek protection.
공시 • Dec 28Vivesto AB's US Clinical Paccal Vet Trial Receives Approval to Start Patient RecruitmentVivesto AB announced that the US Veterinary Review Board Clinical Studies Committee approved the company's planned Paccal Vet open label, pilot clinical study in dogs with splenic hemangiosarcoma following splenectomy. Clinical sites have been chosen and will be ready to start activities after supply of Paccal Vet (investigational veterinary product, IVP) in January. A planned interim analysis is expected in the second half of 2024. The Paccal Vet development program was discussed with FDA earlier this year. No further Agency approval is required prior to study start. The study is an open label, exploratory indication finding study in dogs with different stages of splenic hemangiosarcoma (HSA) following splenectomy. The study will include 4 treatment cycles of Paccal Vet (paclitaxel micellar) and it is planned to investigate 2 cohorts. Each cohort is planned to include a maximum of 23 patients. The study will be conducted at 6 clinical sites in Washington and Oregon. First patients are expected to be dosed in early 2024 and a planned interim analysis is expected in the second half of 2024. If promising activity in either cohort is shown, the study shall be followed by a pivotal study designed to confirm the initial findings of this pilot study and to gather further evidence on the safety and efficacy of Paccal Vet in dogs with splenic hemangiosarcoma. Vivesto's drug candidate Paccal Vet consists of paclitaxel formulated with the company's proprietary XR-17 technology. Vivesto has previously shown good safety of Paccal Vet in the treatment of various types of cancer in dogs. The absence of the solvent cremophor, to which dogs are particularly sensitive, may reduce the risk of serious side effects and death associated to the treatment. Paccal Vet also does not require the addition of human albumin, which when used in dogs can cause hypersensitivity reactions and reduced treatment effectiveness.
공시 • Nov 24Vivesto AB (publ) Announces Composition of Nomination CommitteeIn accordance with the principles for appointing a Nomination Committee, which were adopted at Vivesto AB's Annual General Meeting in 2022, it is hereby announced that the Nomination Committee for the 2024 Annual General Meeting has been appointed, based on the ownership structure as per 30 September 2023. The Nomination Committee for the 2024 Annual General Meeting comprises the following members: Per Arwidsson, appointed by Arwidsro, Håkan Lagerberg, appointed by Mastan AB, and Peter Zonabend, Chairman of the Board of Vivesto. Per Arwidsson has been appointed Chairman of the Nomination Committee.
공시 • Nov 18Vivesto AB, Annual General Meeting, May 23, 2024Vivesto AB, Annual General Meeting, May 23, 2024.
공시 • Nov 17+ 2 more updatesVivesto AB to Report Nine Months, 2024 Results on Nov 21, 2024Vivesto AB announced that they will report nine months, 2024 results on Nov 21, 2024
공시 • Aug 05Vivesto AB Announces Early Termination of Patient Enrollment in the Investigator-Initiated Phase 1B Docetaxel Micellar StudyVivesto AB announced early termination of patient enrollment in the Docetaxel micellar advanced prostate cancer Phase 1b study with the Swiss Group for Clinical Cancer Research (SAKK). The open-label, multicenter, single-stage Phase 1b study has closed its accrual after enrollment of 11 of the planned 18 patients, since Vivesto believes that the data generated will be sufficient ahead of switching into development with a new formulation based on its improved XR-18 micelle technology platform. Docetaxel mousellar has shown good tolerability at doses considered standard for conventional docetaxel formulations, as well as signs of clinical activity. Docetaxel miceLLar has been well received by investigators of the SAKK 67/20 and by participating prostate cancer patients. Vivesto's Docetaxel micellAR is a solvent-free formulation of docetaxel developed to avoid the need for the solubility enhancers in a solvent-based docetaxel and the mandatory high-dose steroid premedication. Patients treated with other existing formulations of docetaxel require steroid administration to avoid certain serious adverse events related to the formulations with solvent. The administration of steroids can lead to marked bone fragility, exacerbated by cancer metastases in the bone, or steroid-related metabolic issues. Vivesto has progressed in the development of its XR-18 drug delivery platform and intends to use this next-generation improved technology in future development of Docetaxel miceller.
공시 • Nov 17+ 3 more updatesVivesto AB to Report Fiscal Year 2023 Results on Feb 23, 2024Vivesto AB announced that they will report fiscal year 2023 results on Feb 23, 2024