Vivesto AB

DUBLIN--( BUSINESS WIRE )--The "Ovarian Cancer Drugs - Global Strategic Business Report" report has been added to ResearchAndMarkets.com's offering. The global market for Ovarian Cancer Drugs is estimated at US$3.5 Billion in 2023 and is projected to reach US$4.8 Billion by 2030, growing at a CAGR of 4.6% from 2023 to 2030. This comprehensive report provides an in-depth analysis of market trends, drivers, and forecasts, helping you make informed business decisions. The growth in the ovarian cancer drugs market is driven by several factors. Increasing awareness and early diagnosis through advanced screening techniques are expanding the patient pool eligible for treatment. Technological advancements in genomics and molecular biology are facilitating the development of targeted therapies and personalized medicine, which are proving to be more effective and have fewer side effects. The substantial investment in research and development by pharmaceutical companies is leading to a robust pipeline of new drugs and combination therapies. Regulatory incentives and expedited approval processes for drugs targeting rare and aggressive cancers are also propelling market growth. Additionally, the rising incidence of ovarian cancer globally, coupled with an aging population, is increasing the demand for effective treatments. Collaborations between academic institutions, research organizations, and pharmaceutical companies are fostering innovation and expediting the translation of research into clinical practice. As these trends continue to evolve, the ovarian cancer drugs market is poised for significant growth, driven by the need for better therapeutic options and the ongoing advancements in cancer treatment. Why You Should Buy This Report: Detailed Market Analysis: Access a thorough analysis of the Global Ovarian Cancer Drugs Market, covering all major geographic regions and market segments. Competitive Insights: Get an overview of the competitive landscape, including the market presence of major players across different geographies. Future Trends and Drivers: Understand the key trends and drivers shaping the future of the Global Ovarian Cancer Drugs Market. Actionable Insights: Benefit from actionable insights that can help you identify new revenue opportunities and make strategic business decisions. Key Insights: Market Growth: Understand the significant growth trajectory of the Targeted Therapy segment, which is expected to reach US$2.9 Billion by 2030 with a CAGR of a 5.5%. The Hormonal Therapy segment is also set to grow at 3.8% CAGR over the analysis period. Regional Analysis: Gain insights into the U.S. market, estimated at $949.5 Million in 2023, and China, forecasted to grow at an impressive 7.8% CAGR to reach $991.3 Million by 2030. Discover growth trends in other key regions, including Japan, Canada, Germany, and the Asia-Pacific. Report Features: Comprehensive Market Data: Independent analysis of annual sales and market forecasts in US$ Million from 2023 to 2030. In-Depth Regional Analysis: Detailed insights into key markets, including the U.S., China, Japan, Canada, Europe, Asia-Pacific, Latin America, Middle East, and Africa. Company Profiles: Coverage of major players such as AbbVie, Inc., Acrivon Therapeutics, AstraZeneca PLC, and more. Complimentary Updates: Receive free report updates for one year to keep you informed of the latest market developments. Key Attributes: Report Attribute Details No. of Pages 250 Forecast Period 2023 - 2030 Estimated Market Value (USD) in 2023 $3.5 Billion Forecasted Market Value (USD) by 2030 $4.8 Billion Compound Annual Growth Rate 4.6% Regions Covered Global MARKET OVERVIEW Influencer Market Insights Global Economic Update Ovarian Cancer Drugs - Global Key Competitors Percentage Market Share in 2024 (E) Competitive Market Presence - Strong/Active/Niche/Trivial for Players Worldwide in 2024 (E) MARKET TRENDS & DRIVERS Increasing Awareness and Early Diagnosis Expand Addressable Market Opportunity Advances in Genomic and Molecular Biology Propel Development of Targeted Therapies Rising Incidence of Ovarian Cancer Drives Demand for Effective Treatments Development of Personalized Medicine Strengthens Business Case for Novel Therapies Growing Adoption of PARP Inhibitors and Other Targeted Therapies Spurs Market Expansion Integration of Immunotherapy in Treatment Protocols Throws Spotlight on Innovative Approaches Expansion of Clinical Trials for Combination Therapies Drives Market Growth Enhanced Screening Techniques and Diagnostic Tools Accelerate Early Detection Rising Healthcare Expenditure and Improved Access to Treatments Expand Market Reach Growing Focus on Reducing Side Effects and Improving Quality of Life Propels Demand for Advanced Therapies Focus on Overcoming Drug Resistance Generates Opportunities for New Treatments Market Penetration in Emerging Economies Propels Growth FOCUS ON SELECT PLAYERS (Total 86 Featured) AbbVie, Inc. Acrivon Therapeutics AstraZeneca PLC Bristol-Myers Squibb Company Daiichi Sankyo Co., Ltd. F. Hoffmann-La Roche AG GSK PLC ImmunoGen, Inc. Imvax Merck & Co., Inc. Ono Pharmaceutical Co., Ltd. Pfizer, Inc. Taiho Pharmaceutical Co., Ltd. Vivesto AB Zymeworks, Inc. For more information about this report visit https://www.researchandmarkets.com/r/euufhd About ResearchAndMarkets.com ResearchAndMarkets.com is the world's leading source for international market research reports and market data. We provide you with the latest data on international and regional markets, key industries, the top companies, new products and the latest trends.

DUBLIN, Dec. 19, 2022 /PRNewswire/ -- The "Cytotoxic Drugs and HPAPI Manufacturing Market by Type of Product, Company Size, Scale of Operation, Type of Molecule, Type of Highly Potent Finished Dosage Form, and Key Geographies, Europe, Asia-Pacific and Rest of the World: Industry Trends and Global Forecasts, 2022-2035" report has been added to ResearchAndMarkets.com's offering. "Cytotoxic Drugs and HPAPI Manufacturing Market 2022-2035" report features an extensive study of the current market landscape and future potential of the HPAPI and cytotoxic drug manufacturing market, over the next decade. The study also features an in-depth analysis, highlighting the capabilities of various industry stakeholders engaged in this field. Aided by the ongoing advancements in clinical pharmacology and oncology research, as well as the rising demand for targeted therapies, high potency active pharmaceutical ingredients (HPAPIs) and cytotoxic drugs have emerged as one of the key areas of interest for researchers and drug developers worldwide. One of the key objectives of the report was to evaluate the current opportunity and the future growth potential of the HPAPI and cytotoxic drug manufacturing market over the coming years. We have provided an informed estimate on the likely evolution of the market in the short to mid-term and long term, for the period 2022-2035. The report also features a likely distribution of the current and forecasted opportunity across important parameters. In order to account for future uncertainties and to add robustness to our model, we have provided three market forecast scenarios, namely conservative, base and optimistic scenarios, representing different tracks of the industry's growth. Frequently Asked Questions What are the current opportunities within the HPAPI and cytotoxic drug market? The cytotoxic drugs and HPAPI manufacturing market is presently considered as one of the most powerful and dynamic sectors of the pharmaceutical industry. At present, more than 40% of the total number of drugs are highly potent in nature. Further, around 60% of the HPAPIs are being developed against oncological indications. Considering the upsurge in demand for novel anti-cancer therapeutics, including antibody-drug conjugates (ADCs), high potency compounds have generated significant interest among several researchers and industry stakeholders. What is the need for contract manufacturing organizations (CMOs) in the HPAPI and cytotoxic drug domain? The manufacturing of highly potent APIs and cytotoxic drugs requires an adequate working environment (to prevent cross contamination within multi-product assets), stringent manufacturing protocols (to comply with the established regulatory standards) and a trained workforce (to satisfactorily handle highly potent materials). In addition, it requires an expensive infrastructure, which is often complex to engineer, install and maintain. As a result, various companies rely on third party service providers to leverage their technologies for manufacturing highly potent and cytotoxic compounds and achieve greater operational flexibility. The inherent expertise of CMOs is believed to be capable of enabling reduction in the time-to-market a product and offer significant cost-benefits. What is the current market landscape and recent trends in the HPAPI and cytotoxic drug contract manufacturing domain? Presently, close to 145 companies have the required capabilities to offer HPAPI and cytotoxic drug manufacturing services across different scales of operation. In addition, several contract service providers are entering into strategic alliances in order to consolidate their presence in this field and enhance their existing capabilities to meet the growing demand for high potency molecules. It is worth mentioning that close to 50% of the expansion activities carried out in this market have been focused on improving the existing manufacturing facilities for highly potent molecules, through the addition of new structures and equipment. What are the key challenges faced by HPAPI and cytotoxic drug CMOs? The primary challenge faced during the manufacturing of highly potent APIs and cytotoxic drugs is related to limiting / altogether preventing cross-contamination of the highly potent molecule with other molecules being produced at the same site. Further, the lack of information related to safe exposure levels and toxicity of new chemical entities can risk the lives of workers and harm the environment. As a result, comprehensive management systems are required for safe handling and containment of highly potent molecules. In addition, proper cleaning techniques and waste treatment systems are extremely essential while producing such compounds. What are the key value drivers in the HPAPIs and cytotoxic drugs contract manufacturing market? The increasing demand for cytotoxic drugs has led to a rise in the number of HPAPIs in the overall pharmaceutical development pipeline. In order to cater to the growing demand for the production of such drug candidates, there is a requirement for safe manufacturing and containment technologies. Even though some pharmaceutical companies have made considerable investments to establish in-house capabilities, the capital-intensive nature and specialized containment requirements make the role of contract manufacturers crucial, specifically for small and mid-sized players. How is the revenue generation potential associated with cytotoxic drugs and HPAPI manufacturing market likely to evolve in the coming years? The cytotoxic drugs and HPAPI manufacturing market is projected to grow at a CAGR of approximately 12% in the coming years. Currently, in terms of type of molecule, the market is likely to be driven by highly potent small molecules. However, this trend is expected to change in the foreseen future, as the demand for highly potent biologics, such as cell and gene therapies, increases further. In addition, in terms of scale of operation, majority share of the contract service revenues is expected to be generated by commercial scale manufacturing operations. Specifically, in terms of geography, the cytotoxic drugs and HPAPI manufacturing market in Asia-Pacific is likely to grow at a relatively faster pace (~13%), in the long term. The report features detailed transcripts of interviews held with the following individuals: Antonella Mancuso and Maria Elena Guadagno (Vice President and Chief Operating Officer and Business Director, BSP Pharmaceuticals) Stacy McDonald and Jennifer L. Mitcham (Ex-Group Product Manager and Ex-Director-Business Development); Abul Khair (Business Development Associate, Catalent) Roberto Margarita (Business Development Director, CordenPharma) Klaus Hellerbrand (Managing Director, ProJect Pharmaceutics) Kevin Rosenthal (Ex-Business Head, Formulations and Finished Products, Alphora research) Mark Wright (Ex-Site Head, Grangemouth, Piramal Healthcare) Allison Vavala (Ex-Senior Manager, Business Development, Helsinn) Valentino Mandelli (Marketing and Sales Manager, Pharma, Cerbios-Pharma) Javier E. Aznarez Araiz (Ex-Business Development, Idifarma) COMPANY COMPETITIVENESS ANALYSIS HPAPI Contract Manufacturers: Company Competitiveness Analysis Highly Potent FDF Contract Manufacturers: Company Competitiveness Analysis HPAPI and Highly Potent FDF Contract Manufacturers: Company Competitiveness Analysis COMPANY PROFILES: HPAPI AND CYTOTOXIC DRUG MANUFACTURERS IN NORTH AMERICA AbbVie Cambrex Catalent Pfizer CentreOne Piramal Pharma Solutions COMPANY PROFILES: HPAPI AND CYTOTOXIC DRUG MANUFACTURERS IN EUROPE Abzena Aenova CARBOGEN AMCIS Hovione Lonza COMPANY PROFILES: HPAPI AND CYTOTOXIC DRUG MANUFACTURERS IN ASIA-PACIFIC AND REST OF THE WORLD Intas Pharmaceuticals Scinopharm STA Pharmaceutical (a WuXi AppTec company) Syngene Teva API LIST OF COMPANIES AND ORGANIZATIONS AbbVie Abzena ACES Pharma Adare Pharma Solutions ADC Biotechnology ADC Therapeutics ADIENNE Pharma and Biotech Aenova AGC Pharma Chemicals (A subsidiary of AGC Group) Agno Pharma AIMEDBIO Ajinomoto Bio-Pharma Services ALB Technology Alcami Alkermes Almac Alphora Research Altasciences Alvogen Amneal Pharmaceuticals AMPAC Fine Chemicals (A SK pharmteco company) Angelini Fine Chemicals (A subsidiary of Angelini Pharma) ANI Pharmaceuticals Antengene ANVI Pharma Aptuit (An Evotec company) Ardena Arevipharma (Acquired by Yonsung Group) Aspen API Astellas Pharma Astorg AstraZeneca Asymchem Laboratories Aurigene Pharmaceutical Services Avra Laboratories (Acquired by Advent International) Baxter BioPharma Solutions Bio-Synthesis BioTechnique BioVectra BiVictriX Therapeutics BOC Sciences Boehringer Ingelheim Bolt Biotherapeutics Boryung Pharmaceutical Bright Peak Therapeutics Bristol Myers Squibb BrYet Health Bryllan BSP Pharmaceuticals Bushu Pharmaceuticals Byondis Cambrex Capsugel (A Lonza company) CARBOGEN AMCIS (A Dishman Carbogen Amcis Group company) Catalent CellMosaic Celon Laboratories Cerbios-Pharma ChemCon ChemPartner CordenPharma CoreRx Creative Biolabs CritiTech Curia Custom Pharmaceutical Services (A part of Dr. Reddy's Laboratories) Cytopharma Daiichi Sankyo Dalton Pharma Services Dipharma Divi's Laboratories DOTTIKON EXCLUSIVE SYNTHESIS EirGen Pharma (Acquired by OPKO Health) Eisai Eli Lilly Enteris BioPharma (A subsidiary of SWK Holdings) Esteve Eurofins Scientific EVER Pharma Excella (Acquired by Fareva) Exelixis Fabbrica Italiana Sintetici Fareva Farmabios (A PharmaZell Group company) Farmhispania Femtogenix Fermion (A subsidiary of Orion) Flamma Formex (A subsidiary of Biotech Investment Group (BIG)) Formosa Laboratories Fresenius Kabi Frontida BioPharm (Acquired by Adare Pharma Solutions) Fujimoto Chemicals GeneQuantum Healthcare Genmab GENTEC PHARMACEUTICAL GROUP Gilead Sciences Glycotope Goodwin Biotechnology GP Pharm GTP Bioways Gustave Roussy Helsinn Advanced Synthesis Heraeus Hovione ICROM Idifarma (Acquired by Ardena) IDT Australia Iksuda Therapeutics ImmunoGen Indena Ind-Swift Laboratories Intas Pharmaceuticals Janssen Biotech Kodiak Sciences Kohlberg Kyongbo Pharmaceutical (A subsidiary of Chong Kun Dang Pharmaceutical) LakePharma Laurus Synthesis LegoChem Biosciences Levena Biopharma (A subsidiary of Sorrento Therapeutics) Lonza Lotus Pharmaceuticals Lubrizol Life Science MabPlex Mac-Chem (A NMS Group Company) Magle Chemoswed Malladi Drugs & Pharmaceuticals Mayne Pharma McSAF MEDICHEM Merck Mersana Therapeutics Metrics Contract Services MilliporeSigma Minafin Minakem (A subsidiary of Minafin) Mitsubishi Tanabe Pharma Mubadala MuseChem Natco Pharma Navrogen NBE-Therapeutics NerPharMa NJ Bio Normon Novartis Novasep Oasmia Pharmaceutical OEP Pharma Olon Oncotec Pharma Produktion Oxford BioTherapeutics Parabolic Drugs Patheon (Acquired by Thermo Fischer Scientific) PCI Pharma Services Pensatech Pharma Pfanstiehl Pfizer Pfizer CentreOne Pharmacare Premium Pharmaceutics International Pharmascience PharmaZell PILA PHARMA Piramal Pharma Solutions PrasFarma Procos (A subsidiary of CBC) ProJect Pharmaceutics Pyxis Oncology Quadira Biosciences Quotient Sciences Recipharm Recro Pharma Regis Technologies RemeGen Richman Chemical SafeBridge Consultants (Acquired by Trinity Consultants) Sai Life Sciences Sanofi Sartorius ScinoPharm Taiwan Seagen Seattle Genetics SEQENS (Acquired by SK Capital Partners) Shionogi Pharma Siegfried Sigma-Aldrich Fine Chemicals (SAFC) (a Sigma-Aldrich company) SK biotek SK Capital Societal CDMO Sofpromed Somatek SOTIO Biotech STA Pharmaceutical (A WuXi AppTec company) Stason Pharmaceuticals Sterling Pharma Solutions Sutro Biopharma Swedish Orphan Biovitrum (SOBI) SWK Holdings Symbiosis Pharmaceutical Services Synaffix Synbias Pharma Syngene Synthon TBD-Biodiscovery Tergus Pharma Teva API TRIO Pharmaceuticals Tubulis University of Goettingen UPM Pharmaceuticals Vectura Veranova VERAXA Biotech VUAB Pharma (A SAFICHEM company) VxP Pharma Wavelength Pharmaceuticals (A subsidiary of SEQENS) WuXi Biologics ZNZ Pharma For more information about this report visit Media Contact: Research and Markets Laura Wood, Senior Manager [email protected] For E.S.T Office Hours Call +1-917-300-0470 For U.S./CAN Toll Free Call +1-800-526-8630 For GMT Office Hours Call +353-1-416-8900 U.S. Fax: 646-607-1907 Fax (outside U.S.): +353-1-481-1716 Logo: SOURCE Research and Markets

While Bend, Oregon is more known for its outdoor amenities and the last remaining Blockbuster Video store, Swiss manufacturing company Lonza has expanded its presence in the area. The expanded facility, called the Early Phase Clinical Manufacturing facility, has added a new facility to its small molecules site that also serves as the company’s center of excellence for bioavailability enhancement and inhaled delivery for its small molecules business unit. The new multimillion-dollar, 13,000-square-foot facility now provides additional capacity for solutions to complex bioavailability challenges in clinical projects and contains seven GMP processing suites. Jason Bertola, the executive director of commercial development at Lonza, said in an email to Endpoints News that the expanded facility will support the early clinical phase development and manufacturing capabilities of particle-engineered intermediates and finished oral drug products. “The early stages of drug development are critical to our business, and we continue to observe strong demand from customers. These fit-for-purpose suites are designed to rapidly advance challenging molecules. The facility is now open and includes spray drying dispersion, dry granulation and a tablet press,” Bertola said. According to Lonza, additional developments are already underway. Toward the end of the year, Lonza anticipates adding a second spray dryer specifically designed for the manufacturing of engineered particles for inhalation as well as encapsulation equipment for encapsulated drug products. Lonza has been strengthening its capabilities recently, expanding its API development and manufacturing labs at a site in Nansha, China last year. Oasmia Pharmaceutical has inked a deal with Lonza to manufacture its ovarian cancer drug candidate Cantrixil there. Also in 2021 , the company laid out a $935 million outlay to build new sites in Visp, Switzerland and Portsmouth, NH, to help grow the company’s biologics portfolio. According to a report from NBC News, pharmacies, US territories and federal agencies wasted 82.1 million vaccine doses from December 2020 through mid-May. The leading culprits were the retail pharmacy chains CVS and Walmart, who were responsible for over a quarter of the doses thrown away in the country in that period, mainly due to the large volume of vaccines they received, according to the NBC report. Other major players that have tossed their vaccines include Health Mart, DaVita, Rite Aid, Publix and Costco. This is not the first time a large batch of vaccine doses has been tossed, as a report detailed in early May that the manufacturer Emergent had to destroy over 400 million doses due to a failure of quality standards at their plant in Maryland. In May , Switzerland announced they were destroying 600,000 doses of Moderna’s Spikevax Covid-19 vaccine as the doses have reached their expiration date. England and Denmark have had to toss over 6.6 million doses combined due to expiration dates hitting or donation efforts failing. The UK-based manufacturer SMC has opened the doors of a new facility in Cambridge, UK. Cambridge Pharma, a subsidiary of SMC and Oval Medical Technologies, is now open to offering pharmaceutical development services. Their new 20,000-square-foot facility at the Cambridge Research Park includes a purpose-built sterile fill-finish facility, a process development laboratory and an analytical laboratory. Services at the facility will include process development and scale-up, sterile fill-finish for clinical trials, QC and stability testing, and QP release of the clinical trial process. “We value pharmaceutical partnerships and continue to expand services in development, manufacturing and analytical testing to help accelerate drug product development,” SMC Group CEO Chetan Patel said in a statement. The company’s sterile fill-finish facility contains two clean rooms designed to support batch sizes from 100 units to 15,000 units in vials, cartridges or syringes. Cambridge Pharma is designed to take a customer’s laboratory-scale formulation and develop a process for clinical trials in Phases I to III, including process development and filling of viscous formulations, suspensions and gels.