Ozmosi | NEO-212 Drug Profile
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NEO-212

Alternative Names: NEO-212, NEO212, NEO 212
Clinical Status: Active
Latest Update: 2025-11-13
Latest Update Note: News Article

Product Description

NEO 212 is novel DNA alkylating agent exhibiting superior activity against breast cancer cells in vitro and intracranial triple-negative tumor growth in vivo. NEO212 is a conjugate of temozolomide (TMZ,) with the natural product perillyl alcohol (POH). NEO 212 causes DNA damage and cell death much more efficiently than TMZ because linkage with POH increased it's biological half-life and thus provided greater opportunity for placement of cytotoxic DNA lesions. (Sourced from: https://drugs.ncats.io/drug/237TB781D9)

Mechanisms of Action: Alkylating agent

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Neonc Technologies
Company Location:
Company CEO:
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for NEO-212

Countries in Clinic: United States

Active Clinical Trial Count: 1

Recent & Upcoming Milestones

Highest Development Phases

Phase 2: Adenocarcinoma|Astrocytoma|Brain Cancer|Carcinoma, Merkel Cell|Cervical Cancer|Colorectal Cancer|Esophageal Cancer|Gastrointestinal Cancer|Glioblastoma|Head and Neck Cancer|Melanoma|Non-Small-Cell Lung Cancer|Renal Cell Carcinoma|Small Cell Lung Cancer|Squamous Cell Carcinoma|Transitional Cell Carcinoma

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT06047379

NEO212-01

P2

Recruiting

Non-Small-Cell Lung Cancer|Glioblastoma|Cervical Cancer|Astrocytoma|Brain Cancer|Gastrointestinal Cancer|Colorectal Cancer|Transitional Cell Carcinoma|Adenocarcinoma|Carcinoma, Merkel Cell|Renal Cell Carcinoma|Esophageal Cancer|Melanoma|Small Cell Lung Cancer|Squamous Cell Carcinoma|Head and Neck Cancer

2026-02-28

62%

2024-11-27

Primary Endpoints|Treatments