Clinical trial · Interventional
PROCLAIM-CX-2009: A Trial to Find Safe and Active Doses of an Investigational Drug CX-2009 for Patients With Selected Solid Tumors
A Phase 1-2, Open-Label, Dose-Finding, Proof of Concept, First-in-Human Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of CX-2009 in Adults With Metastatic or Locally Advanced Unresectable Solid Tumors (PROCLAIM-CX-2009)
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Covid Pandemic; Business Decision to separate Phase 2 to new study
Summary
Brief summary (as posted)
The purpose of this first-in-human study of CX-2009 is to characterize the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD) and antitumor activity of CX-2009 in adult subjects with metastatic or locally advanced unresectable solid tumors. PROCLAIM: PRObody CLinical Assessment In Man CX-2009 clinical trial 001 PROBODY is a trademark of CytomX Therapeutics, Inc
Conditions
Conditions (5)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| Head and Neck Cancer | Malignant Head and Neck Neoplasm | ALIAS | 0.90 |
| Non Small Cell Lung Cancer | Lung Non-Small Cell Carcinoma | ALIAS | 0.90 |
| Ovarian Cancer | Malignant Ovarian Neoplasm | CURATED_EXACT | 0.92 |
| Solid Tumor, Adult | Adult Solid Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| CX-2009 | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (4)
- type
- EXPERIMENTAL
- label
- CX-2009 Monotherapy: 21-Day Dosing Regimen-Escalation
- description
- Dose escalation and determination
- interventionNames
- Drug: CX-2009
- type
- EXPERIMENTAL
- label
- CX-2009 Monotherapy: 21-Day Dosing Regimen-Determination
- description
- Additional enrollment into previously cleared monotherapy dose levels
- interventionNames
- Drug: CX-2009
- type
- EXPERIMENTAL
- label
- CX-2009 Monotherapy: 21-Day Dosing Regimen-Expansion
- description
- Dose expansion
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Histologically confirmed diagnosis of metastatic or locally advanced unresectable tumors 2. Patients demonstrating disease progression after treatment with available therapies that are known to confer clinical benefit, or who are intolerant to treatment, 3. Agreement to provide mandatory archival tissue or fresh biopsy. 4. At least 18 years of age. Exclusion Criteria: 1. Active or chronic corneal disorder, history of corneal transplantation, active herpetic keratitis, and active ocular conditions requiring ongoing treatment/monitoring 2. Serious concurrent illness, including clinically relevant active infection 3. History of or current active autoimmune diseases 4. Significant cardiac disease such as recent myocardial infarction 5. History of multiple sclerosis or other demyelinating disease, Eaton-Lambert syndrome (para-neoplastic syndrome), history of hemorrhagic or ischemic stroke within the last 6 months, or alcoholic liver disease; 6. Non-healing wound(s) or ulcer(s) except for ulcerative lesions caused by the underlying neoplasm; 7. History of severe allergic or anaphylactic reactions to previous monoclonal antibody therapy; 8. Currently receiving anticoagulation therapy with warfarin; 9. Major surgery (requiring general anesthesia) within 3 months prior to dosing.
References
Publications (0)
Data not yet available