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Papilloma refers to a benign growth caused by the human papillomavirus (HPV), which is also the leading cause of cervical cancer. Every two minutes, a woman dies from cervical cancer, with global cases rising alarmingly. Despite routine HPV vaccinations preventing most cases, a high unmet clinical need for advanced therapies persists. Current treatment options, such as surgery or cryotherapy, are often invasive and limited. However, the growing focus on immunotherapies, targeted treatments, and antiviral drugs is set to drive pipeline development. These advancements aim to provide safer, more effective solutions to combat human papillomavirus-related diseases, addressing this critical global health challenge.
The Papilloma Drug Pipeline Insight Report by Expert Market Research gives comprehensive insights into papilloma therapeutics currently undergoing clinical trials. It covers various aspects related to the details of each of these drugs under development for papilloma. The papilloma report assessment includes the analysis of over 100 pipeline drugs and 50+ companies. The papilloma pipeline landscape will include an analysis based on efficacy and safety measure outcomes published for the trials, including their adverse effects on patients suffering from the condition, and alignment with papilloma treatment guidelines to ensure optimal care practices.
The assessment part will include a detailed analysis of each drug, drug class, clinical studies, phase type, drug type, route of administration, and ongoing product development activities related to papilloma.
Papilloma refers to growths caused by the human papillomavirus (HPV), which infects epithelial cells, leading to benign tumors. HPV is transmitted through skin-to-skin contact, and while most infections resolve on their own, some can lead to cervical, anal, or throat cancers. The drug pipeline is focused on developing antivirals, immune-based therapies, and vaccines to prevent and treat HPV-related diseases.
Papilloma treatments include cryotherapy, surgical removal, and laser therapy, which target visible warts. For cervical papilloma, HPV vaccines like Gardasil offer prevention. Antiviral treatments and immune therapies are also being explored to target the virus and reduce recurrence, offering more comprehensive management for patients.
The papilloma drug pipeline addresses the increasing global burden of human papillomavirus-related diseases. In Eastern Europe and Southeast Asia, the prevalence of cervical HPV among women has reached 14%. In India, over 80% of sexually active women are likely to acquire genital HPV by age 50. In the United States, from 2017 to 2021, approximately 47,984 new HPV-associated cancer cases were reported annually. These statistics highlight the urgent need for innovative therapies.
This section of the report covers the analysis of papilloma drug candidates based on several segmentations, including:
By Phase
By Drug Class
By Route of Administration
The report covers phase I, phase II, phase III, phase IV, and early-phase drugs. The coverage includes an in-depth analysis of each drug across these phases. According to EMR analysis, phase II covers a major share of the total papilloma clinical trials.
The drug molecule categories covered under the papilloma pipeline analysis include small molecules, monoclonal antibodies, vaccines, and immunotherapies. The report provides a comparative analysis of the drug classes for each drug in various phases of clinical trials for papilloma.
The EMR papilloma drug report insights include the profile of key companies involved in clinical trials and their drugs under development. Below is the list of a few players involved in Papilloma clinical trials:
This section covers the detailed analysis of each drug under multiple phases, including phase I, phase II, phase III, phase IV, and emerging papilloma drugs. It includes product description, trial ID, study type, drug class, administration mode, and papilloma drug candidates' recruitment status.
The Phase 4 study, sponsored by Labo'Life, aims to evaluate the efficacy of 2LPAPI® in clearing genital high-risk HPV (HR-HPV) infections. This placebo-controlled trial includes an estimated 284 participants and spans a 72-month duration. The study began on October 17, 2020, and is expected to be completed by October 30, 2027, with primary results anticipated by March 2027.
Precigen, Inc. is sponsoring a Phase 3 confirmatory study to assess the efficacy and safety of PRGN-2012 for treating recurrent respiratory papillomatosis (RRP) in adults. This single-arm, open-label trial involves about 42 participants with a history of repeated surgical debulking. The study began on July 11, 2024, and is estimated to complete primary evaluation by March 2027, with completion by March 2029.
The clinical trial, sponsored by Theravectys S.A., aims to evaluate the safety, immunogenicity, and preliminary efficacy of Lenti-HPV-07 immunotherapy for HPV-associated cervical and oropharyngeal cancers. The objective of this Phase 1/2a study is to assess whether Lenti-HPV-07 induces an immune response and its safety profile. The study is expected to be completed by December 2026, with around 72 participants enrolled.
*Please note that this is only a partial list; the complete list of drugs will be available in the full report.*
The Papilloma Drug Pipeline Insight Report provides a strategic overview of the latest and future landscape of treatments for papilloma. It provides necessary information for making informed investment decisions along with research, development, and strategic planning efforts. The stakeholders will benefit from the essential insights into papilloma collaborations, regulatory environments, and potential growth opportunities.
Human Papillomavirus (HPV) Drug Pipeline
Global Human Papillomavirus (HPV) Vaccine Market
Human Papillomavirus-Positive Oropharyngeal Cancer Drug Pipeline
*While we strive to always give you current and accurate information, the numbers depicted on the website are indicative and may differ from the actual numbers in the main report. At Expert Market Research, we aim to bring you the latest insights and trends in the market. Using our analyses and forecasts, stakeholders can understand the market dynamics, navigate challenges, and capitalize on opportunities to make data-driven strategic decisions.*
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Scope of the Report |
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Drug Pipeline by Clinical Trial Phase |
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Route of Administration |
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United States (Head Office)
30 North Gould Street, Sheridan, WY 82801
+1-415-325-5166
Australia
63 Fiona Drive, Tamworth, NSW
+61-448-061-727
India
C130 Sector 2 Noida, Uttar Pradesh 201301
+91-723-689-1189
Philippines
40th Floor, PBCom Tower, 6795 Ayala Avenue Cor V.A Rufino St. Makati City, 1226.
+63-287-899-028, +63-967-048-3306
United Kingdom
6 Gardner Place, Becketts Close, Feltham TW14 0BX, Greater London
+44-753-713-2163
Vietnam
193/26/4 St.no.6, Ward Binh Hung Hoa, Binh Tan District, Ho Chi Minh City
+84-865-399-124
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