Daewoong Therapeutics Microneedle Patch Achieves Best-in-Class Bioavailability, Proving the Strength of Its Drug-Delivery Platform
A potential game changer that addresses both the pain of injections and the low efficiency of oral formulations
In the obesity treatment market, delivery technology is expected to be the decisive factor shaping future leaders
SEOUL, South Korea, Aug. 13, 2025 /PRNewswire/ — Daewoong Pharmaceutical (Co-CEOs Seong-Soo Park and Chang-Jae Lee) and Daewoong Therapeutics (CEO Bok-Ki Kang) announced that their proprietary semaglutide microneedle patch achieved more than 80%relative bioavailability compared to the injectable formulation in a pilot human pharmacokinetic study.
This was based on the healthy volunteer study using semaglutide microneedle patch using Daewoong Therapeutics' CLOPAM® (CLOsed Packed Aero-pressured Microneedle) drug-delivery platform. The study directly compared delivery efficiency with semaglutide subcutaneous injection.
In the trial, 70 healthy adults received single dose of either a semaglutide microneedle patch or a subcutaneous injection. Plasma concentrations were measured and then compared with results from semaglutide subcutaneous injection under the same conditions. After adjusting to equivalent dose, the patch showed more than 80%relative bioavailability compared with injection.
This result is the highest reported for a microneedle patch with the same active ingredient, far exceeding the approximately 30 percent achieved by existing patches. It also showed around 160 times higher bioavailability than semaglutide oral tablet.
Therapeutic plasma levels were maintained for one week, supporting the potential for once-weekly dosing with a single high-load patch. The exposure profile was comparable to that of the injectable counterpart, which strengthens the commercial prospects for a patch-based obesity treatment.
Technology as the Decisive Factor in the Obesity Market
According to Grand View Research, the global obesity therapeutics market is valued at 15.9 billion US dollars in 2024 and is projected to grow to 60.5 billion US dollars by 2030. Currently, therapeutic and safety advantages in the GLP-1 drug class are limited, and experts expect Experts expect delivery technologies improving both bioavailability and patient convenience will be the factor that determines future market leaders. Microneedle patches are attracting attention because they address two key limitations of current therapies: pain of injections and low drug delivery efficiency of oral formulations.
While semaglutide oral tablet is available on the market, it has very low bioavailability and requires complex medication regimen, such as fasting before dosing, limiting water intake, and avoiding co-administration with other drugs for chronic patients potentially lowering adherence. A once-weekly microneedle patch offers a simpler, needle-free option that could be used by a wider range of patients, including those who avoid injections.
Daewoong's Microneedle Technology Innovation Leading the Global Market
The results were made possible by Daewoong Therapeutics' patented CLOPAM® microneedle platform technology, a dissolving-type microneedle technology designed for precise, skin-based drug delivery. The platform uses pressurized drying and hermetic packaging to improve drug uniformity and stability, allowing accurate dosing with minimal contamination risk. CLOPAM® currently has 52 patent filings worldwide and is positioning to be one of Daewoong's leading technologies.
Unlike other injectable products containing semaglutide that require cold-chain storage, Daewoong's patches remain stable at room temperature, which can reduce distribution costs. They also help cut down on medical waste from syringes and needles, aligning with sustainability goals in healthcare.
Based on these results, Daewoong Therapeutics is planning to broaden the collaborative initiatives to the global market via technology licensing, co-development, and out-licensing to prepare for commercialization.
'The microneedle patch must achieve not only high bioavailability but also a drug load sufficient for therapeutic effect,' said Bok-Ki Kang, CEO of Daewoong Therapeutics. 'In this study, we incorporated a high dose of semaglutide into a single patch and showed the potential for once-weekly application. This overcomes a key limitation of previous microneedle approaches and provides a strong foundation for global technology transfer and commercialization.'
'Microneedle formats have long promised better adherence, but high-dose delivery has been a challenge,' said Seong-Soo Park, CEO of Daewoong Pharmaceutical. 'This work is the first to overcome that barrier. We plan to expand microneedle technology to a wide range of biologics to lead the global platform market.'
About Daewoong Pharmaceutical
Daewoong Pharmaceutical (KRX: 069620.KS), established in 1945, is a global pharmaceutical company headquartered in South Korea. The company develops, manufactures, and markets innovative medicines and healthcare solutions with the mission to improve quality of life worldwide. Daewoong specializes in treatments for intractable and rare diseases, supported by in-house research and development, open innovation, and advanced manufacturing capabilities.
Recent achievements include the development and approval of novel drugs for gastroesophageal reflux disease (Fexuprazan) and Type 2 diabetes (Enavogliflozin) in consecutive years. The company is also developing a first-in-class oral anti-fibrotic agent for idiopathic pulmonary fibrosis (Bersiporocin), which has received both orphan drug designation and Fast Track status from the US FDA.
About Daewoong Therapeutics
Daewoong Therapeutics Inc., is a subsidiary of Daewoong Group located in South Korea. The company is focused on developing novel drug delivery systems including the dissolving microneedle platform, CLOPAM®. CLOPAM® is currently being applied to various fields including obesity/metabolic diseases and others with aims to improve patient convenience and medication adherence.
Hashtags
Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles
Malaysian Reserve
an hour ago
- Malaysian Reserve
Medulla Expands Global Footprint with Strategic Launch in Singapore
SINGAPORE, Aug. 14, 2025 /PRNewswire/ — Medulla Communications Pvt. Ltd., one of the world's most awarded healthcare advertising agencies, has announced its expansion into Singapore, establishing a strategic hub to serve the Asia-Pacific region. Known for its expertise in solving healthcare challenges over 15 years, Medulla is looking to create a new super-specialist category as the first digital healthcare advertising agency in Asia. Medulla is one of the rare healthcare-specialist agencies to win the world's biggest awards for both creativity and marketing effectiveness, including Cannes Lions and Effies. This reinforces Medulla's commitment to delivering comprehensive healthcare marketing services across the region, spanning brand strategy, 'brand love' campaigns, performance marketing, healthcare professional communications, CRM, patient support programs, and targeted digital campaigns. 'We've spent 15 years understanding and addressing the world's healthcare challenges, working with brands in APAC through our global team. With our proven healthcare communication capabilities, we're well-positioned to create meaningful impact across the region,' said Praful Akali, Founder and Managing Director of Medulla Communications. Leading Medulla's APAC operations as Managing Partner is Taffy Ledesma, a seasoned executive with extensive experience across healthcare, FMCG, and agency leadership. Taffy's career began client side, working with Johnson & Johnson, Mead Johnson, and Unilever, before he transitioned to agency leadership roles—including Managing Director at DDB Indonesia and Country Head for Indonesia at Hello Health Group. Taffy added, 'My experience on both the client and agency sides of healthcare puts me in a strong position to be a true partner to our clients, ensuring their products and services reach the people they are intended to serve. My focus is on driving commercial effectiveness—and that's what true partnerships achieve.' Medulla has partnered with some global companies including Pfizer, Novartis, Ferring, Mylan, Braintap, and more. Medulla is poised to further its mission of delivering transformative healthcare marketing solutions across new frontiers. About Medulla Communications: Founded by Praful Akali in 2008, Medulla Communications has consistently been recognized as one of the top healthcare agencies globally. The agency has been honoured as the #1 Healthcare Agency of the Year at Cannes Lions in 2016 and secured a top three global ranking for three consecutive years (2015–2017). Medulla has also been ranked as the #4 Most Effective Independent Agency globally by Effies, and the #4 Most Effective Specialist Agency globally by WARC. For media inquiries, please contact: press@ | Website: Photo:
Malaysian Reserve
5 hours ago
- Malaysian Reserve
Parents Urged to Make Kids' Bedtime Screen-Free as National Campaign Launches with NYC Flash Mob
'Screen-Free Sleep' movement takes to the streets to address America's youth sleep crisis NEW YORK, Aug. 14, 2025 /PRNewswire/ — In a bold wake-up call to parents everywhere, the team behind the acclaimed Screenagers documentaries and the 'Away for the Day' campaign launched its latest national initiative on Tuesday, August 12th in NYC: Screen-Free Sleep, a movement to keep kids' bedrooms device-free at night and restore healthy rest to a generation in crisis. To mark the campaign's debut, New Yorkers were treated to an unexpected sight: an entire flash mob of Steve Jobs lookalikes – black turtlenecks, jeans, and all – took to the streets, handing out 'iSleep Pro' kits: sleek, phone-style packaging featuring simple sleep masks as a symbol of unplugged rest. Billed as a 'technological bedtime breakthrough,' the iSleep Pro kits unveiled the real game-changer: no devices in kids' bedrooms at night – a practice the campaign is calling the seatbelt of our time. The message was clear: parents must wake up to the growing crisis – with phones and screens invading bedtime, children are sleeping less, struggling more, and paying the price with their health, mood, and academic performance. 'Sleep is as essential to a child's health as nutrition and exercise,but right now, screens are robbing our kids of it,' said Dr. Delaney Ruston, physician, filmmaker, and co-founder of the Screen-Free Sleep campaign. 'Our campaign empowers parents to make bedrooms device-free at night, building habits that last through the teen years. By making screen-free sleep the norm, we can give our children the rest they need to thrive.' The Alarming Numbers: 1 in 4 tweens sleep with their phone in hand. Kids with devices in their bedroom are 2.3x more likely to feel tired during the day. 51% of teens get fewer than 7 hours of sleep most nights. The Solution: Parents are encouraged to take the pledge at to: Remove all devices – phones, tablets, laptops, smartwatches, gaming devices, even smart speakers – from kids' bedrooms at night. Provide a basic alarm clock to replace phone alarms. Store devices overnight in a secure location (ideally in a parent's bedroom to reduce temptation). Why It Matters: Research shows that simply having a device in the room, even if it's not in use, disrupts kids' sleep. Groundbreaking research shows that sleep deprivation in tweens is associated with MRI-verified disruptions in brain development. A device-free bedroom supports emotional regulation, attention, and school performance. How to Get Involved: Parents can sign the pledge, share the campaign with friends, and bring 'iSleep Pro' kits to schools, sports events, and community gatherings to help normalize screen-free sleep – just as seat belts became standard safety practice. Assets & Interviews Available: Flash Mob & Campaign Photos: HERE Available experts: Dr. Delaney Ruston – Physician, filmmaker, founder of Screenagers & Screen-Free Sleep Judith Owens, MD, MPH, expert in pediatric sleep medicine, Boston Children's Hospital Lauren Hale, Phd, Sleep Expert, Renaissance School of Medicine, NY Dr. Delaney Ruston – Physician, filmmaker, founder of Screenagers & Screen-Free Sleep Judith Owens, MD, MPH, expert in pediatric sleep medicine, Boston Children's Hospital Lauren Hale, Phd, Sleep Expert, Renaissance School of Medicine, NY To learn more, visit For additional details or to arrange interviews, please contact kelly@
Malaysian Reserve
11 hours ago
- Malaysian Reserve
GnRH Antagonists Market on Upward Trajectory During the Forecast Period (2025-2034) Across the 7MM
The GnRH inhibitor market is shifting toward more convenient, patient-focused treatments, driven by oral therapies such as ORGOVYX and YSELTY. As the pipeline continues to grow and indications expand, this drug class is poised for broader clinical use and is likely to play a key role in the future of hormonal suppression in oncology and women's health. LAS VEGAS, Aug. 13, 2025 /PRNewswire/ — DelveInsight's GnRH Receptor Antagonists Market Size, Target Population, Competitive Landscape & Market Forecast report includes a comprehensive understanding of current treatment practices, addressable patient population, which includes top indications such as Endometriosis, fibroids, prostate cancer, and others. The selected indications are based on approved therapies and ongoing pipeline activity. The report also provides insights into the emerging GnRH receptor antagonists, market share of individual therapies, and current and forecasted market size from 2020 to 2034, segmented into 7MM. Key Takeaways from the GnRH Receptor Antagonists Market Report As per DelveInsight's analysis, the total market size of GnRH receptor antagonists in the 7MM is expected to surge significantly by 2034. The report provides the total potential number of patients in the indications, such as Endometriosis, fibroids, prostate cancer, and others. Leading GnRH receptor antagonist companies, such as Debiopharm, Tiumbio, Antev, and others, are developing novel GnRH Receptor Antagonists that can be available in the GnRH receptor antagonist market in the coming years. Some of the key GnRH receptor antagonists in the pipeline include Debio 4326, Merigolix (TU2670), Teverelix, and others. In May 2025, TiumBio and Daewon Pharmaceutical completed Phase II clinical trial of 'Merigolix (TU2670/DW4902)' for Uterine Fibroids with positive results. In March 2025, Kissei initiated the Phase III Clinical Trial for the GnRH Antagonist 'Linzagolix' indicated for Endometriosis in Japan. In February 2025, Kissei submitted New Drug Application (NDA) for 'linzagolix' indicated for Uterine Fibroids in Japan. In the EU, linzagolix received marketing authorization for uterine fibroids in June 2022. Discover which indication is expected to grab the major GnRH receptor antagonists market share @ GnRH Receptor Antagonists Market Report GnRH Receptor Antagonists Market Dynamics The GnRH receptor antagonists market is witnessing steady growth driven by advancements in therapeutic applications across a range of hormone-related disorders. These antagonists function by directly inhibiting GnRH receptors in the pituitary gland, thereby suppressing the release of LH and FSH. This mechanism provides a rapid and reversible suppression of sex hormones such as testosterone and estrogen, making them effective alternatives to GnRH agonists, which are associated with an initial hormone surge. Key indications for GnRH receptor antagonists include prostate cancer, endometriosis, uterine fibroids, and assisted reproductive technologies (ART). One of the significant drivers of market expansion is the growing prevalence of hormone-sensitive cancers, particularly prostate cancer in men and endometriosis or uterine fibroids in women. The increasing demand for therapies with improved safety profiles and faster onset of action has created a favorable environment for GnRH antagonists. Moreover, recent product launches such as RELUGOLIX (marketed as ORGOVYX for prostate cancer and MYFEMBREE for uterine fibroids) and ELAGOLIX (marketed as ORILISSA for endometriosis and ORIAHNN for fibroids) have gained regulatory approvals and demonstrated commercial success, further validating the therapeutic potential of this class. Additionally, the market is benefiting from a broader shift towards oral therapies. Unlike older GnRH agonists, many of the newer antagonists are available in oral formulations, improving patient adherence and convenience. This factor is particularly significant in chronic indications where long-term management is necessary. The preference for non-invasive treatment options among patients and providers is reshaping treatment paradigms and expanding the reach of GnRH antagonists beyond hospital settings to outpatient care. However, the market also faces certain challenges. Cost of therapy remains a barrier in several regions, particularly in low- and middle-income countries, where access to advanced hormonal therapies is limited. Furthermore, competition from alternative treatment modalities such as aromatase inhibitors, progestins, and surgical interventions can restrict market penetration in some indications. Intellectual property protection, regulatory requirements, and long development timelines can also impact new entrants and biosimilar competition. In the coming years, continued R&D in expanding the therapeutic use of GnRH antagonists, including potential applications in breast cancer, male infertility, and transgender hormone therapy, is likely to support further market growth. Strategic collaborations, licensing deals, and increasing investments by pharmaceutical companies in reproductive health and oncology are expected to drive innovation and market competitiveness. Overall, the GnRH receptor antagonists market is positioned for sustained growth, underpinned by clinical efficacy, patient-centric delivery formats, and expanding disease awareness. GnRH Receptor Antagonists Treatment Market The introduction of oral GnRH antagonists, known for their rapid onset of action, is reshaping treatment approaches for several prevalent gynecologic and oncologic conditions such as endometriosis, uterine fibroids, and prostate cancer. Over the past decade, the GnRH inhibitor market has undergone a significant transformation, moving from injectable formulations to more convenient oral therapies. Initially, the market was led by FIRMAGON, an injectable GnRH antagonist approved in 2008 for advanced prostate cancer. However, a major turning point came in 2020 with the approval of ORGOVYX by Sumitomo Pharma—the first oral GnRH antagonist for prostate cancer. ORGOVYX marked a clinical advancement by eliminating the testosterone flare linked with GnRH agonists and improving patient convenience by removing the need for injections. Its rapid adoption in androgen deprivation therapy (ADT) highlighted a growing preference for oral options. Another significant development was the approval of YSELTY (linzagolix) in 2022 by the EMA for treating uterine fibroids and endometriosis. Developed by Theramex and Kissei, YSELTY extended the use of GnRH antagonists into women's health, offering a once-daily oral therapy with customizable suppression levels to help mitigate long-term estrogen deficiency effects. This approval further validated the use of oral GnRH inhibitors beyond oncology and underscored their expanding role in broader therapeutic areas. Learn more about the GnRH receptor antagonists @ GnRH Receptor Antagonists Analysis Key Emerging GnRH Receptor Antagonists and Companies Key players in the GnRH receptor antagonist market include Tiumbio (Merigolix), Antev (Teverelix), Debiopharm (Debio 4326), and others. Debio 4326 is an innovative, injectable, and biodegradable formulation of triptorelin, designed to provide extended-release over 12 months for managing central precocious puberty (CPP). Its key advantage lies in significantly reducing injection frequency, thereby easing the treatment experience for children with this rare condition. Developed based on positive efficacy and safety data from existing 1-, 3-, and 6-month triptorelin products, this new version aims to enhance long-term adherence and minimize the emotional and physical stress on both children and their caregivers. Debio 4326 is currently undergoing a Phase 3 clinical trial across North and South America to assess its efficacy and safety. Teverelix is a long-acting, injectable GnRH antagonist formulated using a novel microcrystal technology that addresses the known safety limitations of earlier GnRH antagonist treatments for prostate cancer. With favorable injection site tolerance and a six-week dosing schedule, Teverelix is positioned to offer better patient compliance and improved treatment outcomes. Beyond prostate cancer, it also holds potential for treating benign prostate hyperplasia (BPH), acute urinary retention (AUR), endometriosis, and uterine fibroids. In January 2023, the U.S. FDA reviewed early-stage clinical data (Phase I and IIa) and provided written feedback on the design of Antev's planned Phase III trial for Teverelix, targeting patients with advanced prostate cancer and high cardiovascular risk—an area with significant unmet clinical need. Subsequently, in December 2023, the FDA approved a Phase IIb trial involving 40 patients with advanced prostate cancer. In November 2024, the agency also approved another Phase IIb study for acute urinary retention, set to enroll 390 patients. These regulatory milestones support Antev's broader strategy to advance Teverelix as a targeted therapy for patients with specific medical needs. The anticipated launch of these emerging therapies are poised to transform the GnRH receptor antagonists market landscape in the coming years. As these cutting-edge therapies continue to mature and gain regulatory approval, they are expected to reshape the GnRH receptor antagonists market landscape, offering new standards of care and unlocking opportunities for medical innovation and economic growth. To know more about GnRH receptor antagonists clinical trials, visit @ GnRH Receptor Antagonists Treatment GnRH Receptor Antagonists Overview GnRH antagonists mark a notable improvement in androgen deprivation therapy (ADT) for treating hormone-sensitive prostate cancer. These drugs function by directly inhibiting GnRH receptors in the pituitary gland, which quickly suppresses the release of luteinizing hormone (LH) and follicle-stimulating hormone (FSH), leading to a rapid drop in testosterone levels. This direct mechanism avoids the initial testosterone surge, or 'flare', that is often seen with other forms of ADT. A major clinical benefit of GnRH antagonists is their swift action, with testosterone levels typically reaching castration thresholds within days. This rapid hormonal suppression is especially beneficial for patients with metastatic or symptomatic disease who require immediate control. Moreover, GnRH antagonists have shown better cardiovascular safety compared to traditional treatments. For instance, the HERO trial demonstrated that relugolix, a once-daily oral GnRH antagonist, significantly reduced the risk of major cardiovascular events. As a result, these agents are particularly advantageous for patients with existing heart-related conditions. GnRH Receptor Antagonists Epidemiology Segmentation The GnRH receptor antagonists market report proffers epidemiological analysis for the study period 2020–2034 in the 7MM, segmented into: Total Cases in Selected Indications for GnRH Receptor Antagonist Total Eligible Patient Pool for GnRH Receptor Antagonist in Selected Indications Total Treated Cases in Selected Indications for GnRH Receptor Antagonist GnRH Receptor Antagonists Report Metrics Details Study Period 2020–2034 GnRH Receptor Antagonists Report Coverage 7MM [The United States, the EU-4 (Germany, France, Italy, and Spain), the United Kingdom, and Japan] Key Indications Covered in the Report Endometriosis, fibroids, prostate cancer, and others Key GnRH Receptor Antagonist Companies Debiopharm, Tiumbio, Antev, Ferring Pharmaceuticals, Sumitomo Pharma, Theramex, Kissei, and others Key GnRH Receptor Antagonists Debio 4326, Merigolix (TU2670), Teverelix, FIRMAGON, ORGOVYX, YSELTY, and others Scope of the GnRH Receptor Antagonists Market Report GnRH Receptor Antagonists Therapeutic Assessment: GnRH Receptor Antagonists' current marketed and emerging therapies GnRH Receptor Antagonists Market Dynamics: Conjoint Analysis of Emerging GnRH Receptor Antagonists Drugs Competitive Intelligence Analysis: SWOT analysis and Market entry strategies Unmet Needs, KOL's views, Analyst's views, GnRH Receptor Antagonists Market Access and Reimbursement Discover more about GnRH receptor antagonists in development @ GnRH Receptor Antagonists Clinical Trials Table of Contents 1 Key Insights 2 Report Introduction 3 Executive Summary of GnRH Receptor Antagonist 4 Key Events 5 Epidemiology and Market Forecast Methodology 6 GnRH Receptor Antagonist Market Overview at a Glance in the 7MM 6.1 Market Share (%) Distribution by Therapies in 2024 6.2 Market Share (%) Distribution by Therapies in 2034 6.3 Market Share (%) Distribution by Indications in 2024 6. Market Share (%) Distribution by Indications in 2034 7 GnRH Receptor Antagonist: Background and Overview 7.1 Introduction 7.2 Treatment 8 Target Patient Pool 8.1 Key Findings 8.2 Assumptions and Rationale: 7MM 8.3 Epidemiology Scenario in the 7MM 8.4 Total Cases in Selected Indications for GnRH Receptor Antagonist in the 7MM 8.5 Total Eligible Patient Pool for GnRH receptor antagonist in Selected Indications in the 7MM 8.6 Total Treated Cases in Selected Indications for GnRH Receptor Antagonist in the 7MM 9 Marketed Therapies 9.1 Key Competitors 9.2 FIRMAGON (degarelix): FERRING PHARMACEUTICALS 9.2.1 Product Description 9.2.2 Regulatory milestones 9.2.3 Other developmental activities 9.2.4 Clinical development 9.2.5 Safety and efficacy 9.3 ORGOVYX (relugolix): Sumitomo Pharma List to be continued in the report 10 Emerging Therapies 10.1 Key Competitors 10.2 Debio 4326: Debiopharm 10.2.1 Product Description 10.2.2 Other developmental activities 10.2.3 Clinical development 10.2.4 Safety and efficacy 10.2.5 Analyst Views 10.3 Teverelix: Antev List to be continued in the report 11 GnRH Receptor Antagonist: Seven Major Market Analysis 11.1 Key Findings 11.2 Market Outlook 11.3 Conjoint Analysis 11.4 Key Market Forecast Assumptions 11.4.1 Cost Assumptions and Rebates 11.4.2 Pricing Trends 11.4.3 Analogue Assessment 11.4.4 Launch Year and Therapy Uptakes 11.5 Total Market Size of GnRH receptor antagonist in the 7MM 11.6 Market Size of GnRH Receptor Antagonist by Indication in the 7MM 11.7 Market Size of GnRH Receptor Antagonist by Therapies in the 7MM 11.8. The United States Market Size 11.8.1 Total Market Size of GnRH Receptor Antagonists in the United States 11.8.2 Market Size of GnRH Receptor Antagonist by Therapies in the United States 11.9 EU4 and the UK Market Size 11.10 Japan Market Size 12 Market Access and Reimbursement 13 SWOT Analysis of GnRH Receptor 14 KOL Views of GnRH Receptor 15 Unmet Needs of GnRH Receptor 16 Bibliography 17 Report Methodology Related Reports Prostate Cancer Market Prostate Cancer Market Insights, Epidemiology, and Market Forecast – 2034 report delivers an in-depth understanding of the disease, historical and forecasted epidemiology, as well as the market trends, market drivers, market barriers, and key prostate cancer companies, including Sanofi, AstraZeneca, Astellas Pharma, Bayer, Novartis, Curium, Merck, Orion, Janssen Pharmaceutical, Pfizer, Exelixis, Ipsen Pharma, Takeda, AB Science, Lantheus, Eli Lilly, POINT Biopharma, Telix Pharmaceuticals, Tavanta Therapeutics, Jiangsu Hengrui Pharmaceuticals, Kangpu Biopharmaceuticals, Fusion Pharma, Merus, Bristol-Myers Squibb, Syntrix Pharmaceuticals, Promontory Therapeutics, Xencor, Taiho Pharmaceutical, Madison Vaccines, MacroGenics, Zenith Epigenetics, Modra Pharmaceuticals, Arvinas, Laekna Therapeutics, Blue Earth Therapeutics, Oncternal Therapeutics, Essa Pharma, Clarity Pharmaceuticals, BioNTech, DualityBio, Daiichi Sankyo, Fortis Therapeutics, ORIC Pharmaceuticals, Amgen, among others. Prostate Cancer Pipeline Prostate Cancer Pipeline Insight – 2025 report provides comprehensive insights about the pipeline landscape, pipeline drug profiles, including clinical and non-clinical stage products, and the key prostate cancer companies, including Curium, Merck, Telix Pharmaceuticals, Exelixis, AstraZeneca, AB Science, Lantheus, Pfizer, Jiangsu Hengrui Pharmaceuticals, Modra Pharmaceuticals, Bristol-Myers Squibb, MacroGenics, Syntrix Pharmaceuticals, Zenith Epigenetics, Xencor, Bristol Myers Squibb, Merus, Phosplatin Therapeutics, Laekna Therapeutics, Tavanta Therapeutics, Madison Vaccines, Taiho Pharmaceutical, Kangpu Biopharmaceuticals, Arvinas, Candel Therapeutics, Blue Earth Therapeutics, Ipsen Biopharmaceuticals, LAVA Therapeutics, Essa Pharma, Poseida Therapeutics, Janux Therapeutics, Aurigene Oncology, Sathgen Therapeutics, Full-Life Technologies, NextPoint Therapeutics, AbbVie, SL VAXiGEN, Sorrento Therapeutics, Inc., 858 Therapeutics, Avacta Life Sciences Ltd, Nammi Therapeutics, BeiGene, DualityBio, among others. Endometriosis Market Endometriosis Market Insights, Epidemiology, and Market Forecast – 2034 report delivers an in-depth understanding of the disease, historical and forecasted epidemiology, as well as the market trends, market drivers, market barriers, and key endometriosis companies, including Mitsubishi Tanabe Pharma America, Ferring Pharmaceuticals, AbbVie, Neurocrine Biosciences, ObsEva, Kissei Pharmaceuticals, SWK, Enteris BioPharma, Bayer, Hope Medicine, Organon, among others. Uterine Fibroids Market Uterine Fibroids Market Insights, Epidemiology, and Market Forecast – 2034 report delivers an in-depth understanding of the disease, historical and forecasted epidemiology, as well as the market trends, market drivers, market barriers, and key uterine fibroids companies, including AbbVie Inc., Addex Therapeutics Ltd, Bayer AG, BioSpecifics Technologies Corp, Dongkook Pharmaceutical Co Ltd, Kissei Pharmaceutical Co Ltd, Myovant Sciences, Ogeda SA, Repros Therapeutics Inc., Takeda Pharmaceutical Company Ltd, among others. About DelveInsight DelveInsight is a leading Business Consultant and Market Research firm focused exclusively on life sciences. It supports pharma companies by providing comprehensive end-to-end solutions to improve their performance. Get hassle-free access to all the healthcare and pharma market research reports through our subscription-based platform PharmDelve. Contact UsShruti Thakur info@ +14699457679 Logo: View original content:
