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| Share Name | Share Symbol | Market | Type |
|---|---|---|---|
| Morphosys AG | TG:MOR | Tradegate | Ordinary Share |
| Price Change | % Change | Share Price | Bid Price | Offer Price | High Price | Low Price | Open Price | Shares Traded | Last Trade | |
|---|---|---|---|---|---|---|---|---|---|---|
| 0.00 | 0.00% | 68.10 | 68.10 | 68.10 | 0.00 | 01:00:00 |
From Jun 2023 to Jun 2024
By Ben Glickman
MorphoSys said its study of a treatment for myelofibrosis, a rare form of blood cancer, reached its primary endpoint, clearing the way for a new drug application in mid-2024.
The German pharmaceutical company said Monday its Phase 3 trial of pelabresib in combination with ruxolitinib in myelofibrosis patients found a statistically significant and clinically meaningful improvement in the portion of patients with a 35% or greater reduction in spleen volume after 24 weeks.
There was also a meaningful reduction in myelofibrosis symptoms, a key secondary endpoint, according to the company.
MorphoSys now intends to submit a new drug application for pelabresib in combination with ruxolitinib to U.S. and European regulators in mid-2024.
The company's combination therapy received fast track designation from the Food and Drug Administration in treating myelofibrosis in 2018.
Write to Ben Glickman at ben.glickman@wsj.com
(END) Dow Jones Newswires
November 20, 2023 17:04 ET (22:04 GMT)
Copyright (c) 2023 Dow Jones & Company, Inc.
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