Clinical trial · Interventional
Aurora Kinase Inhibitor AT9283 in Treating Patients With Advanced or Metastatic Solid Tumors or Non-Hodgkin's Lymphoma
A Phase I Study of AT9283 Given As a 24 Hour Infusion on Days 1 and 8 Every Three Weeks in Patients With Advanced Incurable Malignancy
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
RATIONALE: Aurora kinase inhibitor AT9283 (AT9283) may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. PURPOSE: This phase I trial is studying the side effects and best dose of AT9283 in treating patients with advanced or metastatic solid tumors or non-Hodgkin's lymphoma.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Non-Hodgkins Lymphoma | Non-Hodgkin Lymphoma | ALIAS | 0.90 |
| Unspecified Adult Solid Tumor, Protocol Specific | Adult Solid Neoplasm | ALIAS | 0.85 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Aurora kinase inhibitor AT9283 | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- AT9283
- interventionNames
- Drug: Aurora kinase inhibitor AT9283
Primary outcomes (4)
- measure
- Maximum tolerated dose of Aurora kinase inhibitor AT9283 (AT9283)
- timeFrame
- 1 year
- description
- Doses escalated as described in protocol section 4.3. MTD defined as that dose at which ≥ 2/6 or ≥ 2/3 patients experience DLT (as defined in protocol section 4.4).
- measure
- Recommended phase II dose of AT9283
- timeFrame
- 1 year
- description
- RPTD defined as one dose lower than MTD.
- measure
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
DISEASE CHARACTERISTICS: * Histologically or cytologically confirmed diagnosis of 1 of the following: * Advanced and/or metastatic solid tumor * Advanced or metastatic non-Hodgkin's lymphoma refractory to standard therapy * Clinically or radiologically documented disease * No tumor marker elevation as only evidence of disease * No untreated brain or meningeal metastases * Treated and stable brain metastases allowed provided they are asymptomatic and do not require steroids PATIENT CHARACTERISTICS: * ECOG performance status 0-2 * Absolute granulocyte count ≥ 1,500/mm³ * Platelet count ≥ 100,000/mm³ * Creatinine ≤ 1.25 times upper limit of normal (ULN) OR creatinine clearance ≥ 50 mL/min * Bilirubin normal * ALT and AST ≤ 2 times ULN (≤5 times ULN if liver metastases are present) * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use two effective methods of contraception * No untreated or uncontrolled hypertension, cardiovascular conditions, or symptomatic cardiac dysfunction * No active or uncontrolled infections * No serious illness or medical condition that would preclude study treatment PRIOR CONCURRENT THERAPY: * At least 2 weeks since prior major surgery and recovered * At least 3 weeks since prior palliative radiotherapy and recovered * Low-dose, nonmyelosuppressive radiotherapy may be allowed * At least 3 weeks since prior chemotherapy for solid tumors and recovered * No more than 2 prior cytotoxic chemotherapy regimens for metastatic disease * At least 4 weeks since prior steroids * No limitations on prior therapy for patients with non-Hodgkin's lymphoma * Prior hormonal, immunologic, biologic or signal transduction inhibitor therapy allowed * No other concurrent investigational agents * No other concurrent anticancer therapy
References
Publications (1)
- RESULTDent SF, Gelmon KA, Chi KN, Jonker DJ, Wainman N, Capier CA, Chen EX, Lyons JF, Seymour L. NCIC CTG IND.181: phase I study of AT9283 given as a weekly 24 hour infusion in advanced malignancies. Invest New Drugs. 2013 Dec;31(6):1522-9. doi: 10.1007/s10637-013-0018-9. Epub 2013 Sep 27. PMID 24072436