Site icon pharmaceutical daily

2021 Report on the Anti-CD30 Therapies Pipeline – Players Include Seagen, Takeda Oncology & Cellular Biomedicine Among Others – ResearchAndMarkets.com

DUBLIN–(BUSINESS WIRE)–The “Anti-CD30 Therapies – Pipeline Insight, 2021” drug pipelines has been added to ResearchAndMarkets.com’s offering.

This report provides comprehensive insights about 10+ companies and 10+ pipeline drugs in Anti-CD30 therapies pipeline landscape. It covers the pipeline drug profiles, including clinical and nonclinical stage products. It also covers the therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space.

Report Highlights

Anti-CD30 therapies Emerging Drugs Chapters

This segment of the Anti-CD30 therapies report encloses its detailed analysis of various drugs in different stages of clinical development, including phase III, II, I, preclinical and Discovery. It also helps to understand clinical trial details, expressive pharmacological action, agreements and collaborations, and the latest news and press releases.

Anti-CD30 therapies Emerging Drugs

Brentuximab vedotin – Seagen/Takeda

Brentuximab Vedotin (ADCETRIS) is an antibody-drug conjugate (ADC) therapy developed by Seagen and its Takeda Oncology. The ADC contains an anti-CD30 monoclonal antibody attached by a protease-cleavable linker to a microtubule disrupting agent, monomethyl auristatin E (MMAE), utilizing Seattle Genetics’ proprietary technology. This linker system makes the molecule stable in the bloodstream but to release MMAE upon internalization into CD30-expressing cells. Under the terms of the collaboration agreement, Seattle Genetics has U.S. and Canadian commercialization rights and Takeda has rights to commercialize ADCETRIS in the rest of the world.

AFM13: Affimed

AFM13 is a tetravalent bispecific chimeric (anti-human CD30 x anti-human CD16A) recombinant antibody construct which is being developed to treat CD30-positive malignancies. The molecule is currently in Phase II clinical evaluation for the treatment of Relapsed/Refractory CD30-positive T-cell Lymphoma or Transformed Mycosis Fungoides.

Anti-CD30 therapies: Therapeutic Assessment

This segment of the report provides insights about the different Anti-CD30 therapies drugs segregated based on following parameters that define the scope of the report.

Major Players working on Anti-CD30 therapies

There are approx. 10+ key companies which are developing the Anti-CD30 therapies. The companies which have their Anti-CD30 therapies drug candidates in the most advanced stage, i.e. Phase III include Seagen/Takeda.

The report covers around 10+ products under different phases of clinical development like

Anti-CD30 therapies pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs such as

Products have been categorized under various Molecule types such as

The drugs have been categorized under various product types like Mono, Combination and Mono/Combination.

Anti-CD30 therapies: Pipeline Development Activities

The report provides insights into different therapeutic candidates in phase III, II, I, preclinical and discovery stage. It also analyses Anti-CD30 therapies therapeutic drugs key players involved in developing key drugs.

Pipeline Development Activities

The report covers the detailed information of collaborations, acquisition and merger, licensing along with a thorough therapeutic assessment of emerging Anti-CD30 therapies drugs.

Anti-CD30 therapies Report Insights

Anti-CD30 therapies Report Assessment

Key Questions Answered

Current Scenario and Emerging Therapies:

Key Players

For more information about this drug pipelines report visit https://www.researchandmarkets.com/r/hi17s7

Contacts

ResearchAndMarkets.com

Laura Wood, Senior Press Manager

press@researchandmarkets.com
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

Exit mobile version