Phase 1 study assessing safety and pharmacokinetic of Chrysalin™ (Rusalatide Acetate, TP508)

Status: Planning

Phase of Trial: Phase I

Latest Information Update: 28 Sep 2023

Price :

$35 ^*

Note:

Adis is an information provider.
Final gross price and currency may vary according to local VAT and billing address.
Your purchase entitles you to full access to the information contained in our trial profile at the time of purchase.
A link to download a PDF version of the trial profile will be included in your email receipt.

At a glance

28 Sep 2023 New trial record
26 Sep 2023 According to Chrysalis media release, the US Food and Drug Administration (FDA) has given the company permission to initiate human clinical trials aimed at treating acute lung failure. With approval of its Investigational New Drug (IND) Application, Chrysalis plans to initiate a Phase 1, Safety and Pharmacokinetic (PK) study for use of TP508 as an injectable drug by year-end and testing of the drug in patients with Acute Respiratory Distress Syndrome (ARDS) in 2024.

If your organization or you do not have a subscription, try one of the following:

Contacting your organization’s admin about adding this content to your AdisInsight subscription
Buying a PDF version of any individual profile
Request a free trial

If your organization has a subscription, there are several access options, even while working remotely:

Working within your organization’s network
Login with username/password or try to access via your institution
Persisted access using your organization’s identifier stored in your user browser for 90 days

For assistance, contact us at asktheexpert.adisinsight@springer.com