Last update 07 Mar 2026

TI-061

Overview

Basic Info

Drug Type
Monoclonal antibody
Synonyms
TI 061, TI061
Target
CD47
Action
inhibitors
Mechanism
CD47 inhibitors(Cluster of differentiation 47 inhibitors)
Therapeutic Areas
NeoplasmsHemic and Lymphatic Diseases
Active Indication-
Inactive Indication
Advanced cancerHematologic NeoplasmsMalignant Solid Neoplasm+ [1]
Originator Organization
Arch Oncology, Inc.Arch Oncology, Inc.
Active Organization-
Inactive Organization
Arch Oncology, Inc.Arch Oncology, Inc.
License Organization-
Drug Highest PhaseDiscontinuedPhase 1/2
First Approval Date-
Regulation-
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Structure/Sequence

Related

1
Clinical Trials associated with TI-061
EUCTR2016-004372-22-GB
/ TerminatedPhase 1/2
A Phase 1-2 Study of Ti-061 Alone and in combination with other anti-cancer agents in Patients with Advanced Malignancies
100 Clinical Results associated with TI-061
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100 Translational Medicine associated with TI-061
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100 Patents (Medical) associated with TI-061
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100 Deals associated with TI-061
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R&D Status

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IndicationHighest PhaseCountry/LocationOrganizationDate
Advanced cancerPhase 2
United Kingdom
-29 Mar 2017
Hematologic NeoplasmsPhase 2
United Kingdom
-29 Mar 2017
Malignant Solid NeoplasmPhase 2
United Kingdom
-29 Mar 2017
Solid tumorPhase 2
United Kingdom
Arch Oncology, Inc.Arch Oncology, Inc.
-
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

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Translational Medicine

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Deal

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Core Patent

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Clinical Trial

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Approval

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Biosimilar

Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.
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Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.

Regulation

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