Ozmosi | INT-2104 Drug Profile
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INT-2104

Alternative Names: INT-2104, INT2104, INT 2104
Clinical Status: Active
Latest Update: 2025-08-21
Latest Update Note: News Article

Product Description

The compelling preclinical findings of specificity, biologic effect, tolerability and pharmacologic profile in multiple animal models following intravenous administration support the advancement of INT2104 to the clinic as a promising treatment option for B-cell malignancies," says Tim Culp, PhD, VP of Research and Development. "We continue to maintain our timeline to IND with initial human data expected in 2024. (Sourced from: https://www.benzinga.com/pressreleases/23/06/n32940039/interius-biotherapeutics-highlights-strong-preclinical-data-supporting-in-vivo-chimeric-antigen-re)

Mechanisms of Action: CAR-T, CD20

Novel Mechanism: Yes

Modality: In Vivo CAR-T

Route of Administration: N/A

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Interius
Company Location: Eastern America
Company Founding Year: None
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for INT-2104

Countries in Clinic: Australia

Active Clinical Trial Count: 1

Recent & Upcoming Milestones

Highest Development Phases

Phase 1: B-Cell Leukemia|Lymphoid Leukemia|Lymphoma, B-Cell|Lymphoma, Non-Hodgkin|Precursor B-Cell Lymphoblastic Leukemia-Lymphoma|Precursor Cell Lymphoblastic Leukemia-Lymphoma

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT06539338

INVISE

P1

Recruiting

Precursor Cell Lymphoblastic Leukemia-Lymphoma|Precursor B-Cell Lymphoblastic Leukemia-Lymphoma|B-Cell Leukemia|Lymphoma, B-Cell|Lymphoid Leukemia|Lymphoma, Non-Hodgkin

2028-03-01

50%

2025-07-30

Patient Enrollment|Primary Endpoints|Start Date|Treatments