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Postion:Product Catalog >API>Hormones and the Endocrine System>Pancreatic hormone and blood sugar regulation>Flibanserin
Flibanserin
  • Flibanserin
  • Flibanserin
  • Flibanserin

Flibanserin

Price $800
Package 1Kg/Bag
Min. Order: 100g
Supply Ability: 5000kg
Update Time: 2021-07-08

Product Details

Product Name: Flibanserin CAS No.: 167933-07-5
EC-No.: 643-002-2 Min. Order: 100g
Purity: 99% Supply Ability: 5000kg
Release date: 2021/07/08
Appearance: White pwoder

Article illustration

Article illustration

Flibanserin HCL (INN, USAN) (developmental code name BIMT-17; proposed trade names Girosa and Addyi) is a drug that is being studied as a non-hormonal treatment for pre-menopausal women with hypoactive sexual desire disorder (HSDD). 

 
Certification of Analysis

 Test Items

      Test Specifications

 Test Results

Appearance

      An off-white to white powder

 Complied

Identification

       Meet the requirements

 Positive

Loss on Drying 

              ≤0.50%

   0.13%

Heavy Metals

              ≤20PPM

   <20PPM

Purity (by HPLC)

               ≥99.0%

    99.2%

Conclusion:

          Conform to standard


 

Article illustration

Flibanserin is used for hypoactive sexual desire disorder among women. Those receiving flibanserin report a 0.5 increase compared to placebo in the number of times they had "satisfying sexual events".In those on flibanserin it rose from 2.8 to 4.5 times a month while women receiving placebo reported also an increase of "satisfying sexual events" from 2.7 to 3.7 times a month.The onset of the flibanserin effect was seen from the first timepoint measured after 4 weeks of treatment and maintained throughout the treatment period.

The effectiveness of flibanserin was evaluated in three phase 3 clinical trials. Each of the three trials had two co-primary endpoints, one for satisfying sexual events (SSEs) and the other for sexual desire. Each of the 3 trials also had a secondary endpoint that measured distress related to sexual desire. All three trials showed that flibanserin produced an increase in the number of SSEs and reduced distress related to sexual desire. The first two trials used an electronic diary to measure sexual desire, and did not find an increase. These two trials also measured sexual desire using the Female Sexual Function index (FSFI) as a secondary endpoint, and an increase was observed using this latter measure. The FSFI was used as the co-primary endpoint for sexual desire in the third trial, and again showed a statistically significant increase.

Article illustration

Article illustration

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