Create Account
Log In
Dark
chart
exchange
Premium
Terminal
Screener
Stocks
Crypto
Forex
Trends
Depth
Close
Check out our Dark Pool Levels


Theravance Biopharma, Inc. (TBPH), a biopharmaceutical company primarily focused on organ-selective medicines, announced Monday that its Phase 2 study of 3 mg once-daily nezulcitinib did not meet the primary endpoint.


RTTNews | Jun 21, 2021 06:32AM EDT

06:32 Monday, June 21, 2021 (RTTNews.com) - Theravance Biopharma, Inc. (TBPH), a biopharmaceutical company primarily focused on organ-selective medicines, announced Monday that its Phase 2 study of 3 mg once-daily nezulcitinib did not meet the primary endpoint.

Nezulcitinib, also known as TD-0903, is an investigational, inhaled, lung-selective, pan-Janus kinase or JAK inhibitor in development for hospitalized patients with confirmed COVID-19 associated acute lung injury and impaired oxygenation.

In pre-market activity on Nasdaq, Theravance shares were losing around 12 percent to trade at $15.51.

In its statement, the company announced top-line results from its Phase 2 study of 3 mg once-daily nezulcitinib compared to placebo, each in combination with standard of care.

The company noted that it was the first investigation of an inhaled JAK inhibitor in COVID-19 patients.

The study was a 1:1 randomized, double-blind, placebo-controlled, multi-center Phase 2 trial for the treatment of hospitalized COVID-19 patients with impaired oxygenation (NCT04402866). Key endpoints were measured through Day 28. Standard of care in the study included approximately 99% receiving steroids (91% received dexamethasone).

Rick Winningham, Chief Executive Officer, Theravance Biopharma, said, "Since learning of the extensive respiratory complications in severe COVID-19, we have worked to advance the science behind inhaled lung-selective JAK inhibitors in critical diseases like COVID-19. Even though this Phase 2 study, enrolling more than 200 patients, did not meet the primary endpoint, we are encouraged by the trend in the pre-specified analysis of the 28-day mortality rate in the intent-to-treat population."

The company said Nezulcitinib demonstrated a favorable trend in improvement when compared to placebo for 28-day all-cause mortality rate. Nezulcitinib was well-tolerated when administered once-daily for up to seven days.

The company said it will share these results with FDA and other regulatory agencies to seek input on protocols to further study nezulcitinib in acute hyperinflammation in the lung.

Read the original article on RTTNews ( https://www.rttnews.com/3203651/theravance-phase-2-nezulcitinib-study-did-not-meet-primary-goal-in-acute-lung-injury-due-to-covid-19.aspx)

For comments and feedback: contact editorial@rttnews.com

Copyright(c) 2021 RTTNews.com All Rights Reserved






Share
About
Pricing
Policies
Markets
API
Info
tz UTC-4
Connect with us
ChartExchange Email
ChartExchange on Discord
ChartExchange on X
ChartExchange on Reddit
ChartExchange on GitHub
ChartExchange on YouTube
© 2020 - 2026 ChartExchange LLC