Either you have JavaScript disabled or your browser does not support Javascript . To work properly, this page requires JavaScript to be enabled.
How to enable JavaScript in your browser?

A Phase 1/2, Open-Label, First-in-human, Multiple Ascending Dose Multicenter Study of MT-101 in Subjects With CD5+ Relapsed/Refractory T Cell Lymphoma

X
Trial Profile

A Phase 1/2, Open-Label, First-in-human, Multiple Ascending Dose Multicenter Study of MT-101 in Subjects With CD5+ Relapsed/Refractory T Cell Lymphoma

Status: Suspended
Phase of Trial: Phase I/II

Latest Information Update: 20 Nov 2023

Price : $35 *
  • 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

  • Drugs MT-101 (Primary) ; Cyclophosphamide; Fludarabine
  • Indications Cutaneous T-cell lymphoma; Peripheral T-cell lymphoma
  • Focus Adverse reactions; First in man
  • Acronyms IMAGINE
  • Sponsors Myeloid Therapeutics
  • Most Recent Events

    • 09 Nov 2023 Planned End Date changed from 1 Oct 2024 to 1 Oct 2025.
    • 09 Nov 2023 Planned primary completion date changed from 1 Nov 2023 to 1 Nov 2024.
    • 09 Nov 2023 Status changed from recruiting to suspended.

You need to be a logged in or subscribed to view this content Request demo

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
  • with username/password or try to via your institution
  • Persisted access using your organization’s identifier stored in your user browser for 90 days
Back to top