1. What is the Chemxpert database?

Chemxpert database is a techno-commercial information platform developed and operated by Lifescience Intellipedia Pvt. Ltd. Our data provides valuable insights regarding sourcing, marketing, development, and regulatory functions for the entire Lifescience industry. The different industries covered by our data encompass APIs, FDFs, pharma intermediates, paints, dyes, polymers, biotechnology, biochemical, food additives, nutraceuticals, etc.

2. How can I subscribe to the Chemxpert database?

You can gain access to the Chemxpert database after subscribing to it by visiting this link: - https://chemxpert.com/pricing

3. How many countries' data is available on your portal?

The Chemxpert database covers more than 200 countries. We are working in the direction of expanding our data coverage in more countries.

4. What are the different sources you use for obtaining information?

The different sources we use for data collection are as follows: - • Primary researc • DMF, ANDA, & CEP list • Conferences, Exhibitions, & Tradeshow • Company annual reports • DMF, ANDA, & CEP list • Subject matter experts & KOL survey. Apart from these, our other valuable sources include application-wise manufacturers list, subscribed and non-subscribed databases, corporate partners, US FDA Orange book, publicly available sources, industry associates, national statistics, regulatory websites, etc. You can gain access to the Chemxpert database after subscribing to it by visiting this link: -https://chemxpert.com/sources

5. What is the expected time for account activation?

Your Chemxpert account will be activated instantly if the payment is made through our website. If you choose to use RTGS, NEFT, or IMPS systems for payment, your account will be activated within 24 hours.

01 Jul 2022
Admin
News Article

Takeda Takhzyro

Children Ages 2 To <12 Experienced 94.8% Fewer Hereditary Angioedema (Hae) Attacks During Treatment With Takhzyro Over The 52-Week Treatment Period Compared To BaselineLate-Breaking Flash Talk Presentation Of Phase 3 Data Highlights Positive, Clinically Meaningful Results In Children <6 Years, Where No Long-Term Prophylaxis Treatment (Ltp) Is Currently ApprovedResults Are Consistent With The Favorable Efficacy And Safety Profile Of Takhzyro Observed In Adult And Adolescent Patients In Earlier StudiesGlobal Regulatory Filings To Begin In Fiscal Year 2022Takeda Today Announced Late-Breaking Data From The Phase 3 Spring Study (Nct04070326) Presented At The European Academy Of Allergy And Clinical Immunology (Eaaci) Hybrid Congress 2022, Demonstrating Positive Results Of Takhzyro

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