Safety and Tolerability of ODM-203 in Subjects With Advanced Solid Tumours (KIDES-203)

Orion Pharma

Status and phase

Completed

Phase 1

Conditions

Solid Tumours

Treatments

Drug: ODM 203

Study type

Interventional

Funder types

Industry

Identifiers

NCT02264418

3113001

Details and patient eligibility

About

The purpose of this first-in-human study is to evaluate the safety and tolerability of escalating doses of ODM-203 in subjects with advanced solid tumours and to determine the maximum tolerated dose and dose limiting toxicities.

Full description

The safety profile of ODM-203 will be explored together with the pharmacokinetics, pharmacodynamics and tumour response to treatment with ODM-203 to recommend the dosing regimen for further clinical studies. The pharmacokinetic properties of ODM 203 will be evaluated after single and multiple dose administrations at different dose levels

Enrollment

84 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Written informed consent
Male and female subjects over 18 years of age
Subjects with histologically or cytologically confirmed locally advanced or metastatic tumours. Subjects in Part 2 to have a tumour/genetic aberration.
Availability of tumour sample for genetic analysis
Adequate haemopoietic, hepatic and renal function
Eastern Cooperative Oncology Group performance status of 0 to 1
Serum mineral levels phosphate: 2.5 mg/dl; calcium: 8.8 mg/dl; magnesium: 1.2 mg/dl; potassium: 11.7 mg/dl; sodium: 299mg/dl.
Recovery from reversible adverse events of previous systemic anti-cancer therapies to baseline or grade 1 with the exception of alopecia;stable neuropathy of grade 2 induced by previous cancer treatment
Life expectancy of 12 weeks or more

Exclusion criteria

Any prior anti VEGFR/FGFR treatment related AE that in the judgement of the investigator is considered severe/life threatening
Subjects receiving warfarin
Active central nervous system metastases not controlled by prior surgery/radiotherapy and/or low dose steroids for 4 weeks or more
Subjects with current evidence of endocrine alteration of calcium-phosphate homeostasis
Concomitant therapies known to increase serum phosphorus and/or calcium levels that cannot be discontinued or switched to a different therapy are not permitted within 14 days before the first dose of ODM-203.
Significant cardiovascular conditions/circumstances as follows:
a active or unstable cardio/cerebro-vascular disease
b Uncontrolled hypertension (systolic blood pressure ≥ 150mmHg and/or diastolic blood pressure ≥ 90mg Hg with optimised antihypertensive therapy.
c history of severe arrhythmia, familial arrhythmia, conduction abnormality or congenital long QT syndrome
dConcomitant therapies known to prolong the QT interval and associated with a risk of Torsades de Pointes are not permitted within 7 days before the first dose of ODM 203
e Repeatable prolongation of QTcF interval ≥ 450 msec or any clinically significant abnormality in the ECG at screening in 2 out of 3 recordings
f Left ventricular ejection fraction <50% at screening
Subjects who received systemic anticancer treatment prior to the first dose of ODM-203 within the following timeframes: less than 28 days since the last dose of antineoplastic therapy and/or 28 days of wide field radiotherapy or 14 days of limited field radiation for palliation
Major surgery or serious infection within 21 days of the first dose of ODM-203
Known gastrointestinal disease or a procedure that may affect absorption of ODM 203
Serious concurrent medical condition or psychiatric illness
History and/or current evidence of ectopic mineralisation/calcification
Known active or past history of other primary malignancy
Female of child bearing potential
Female of child bearing potential or male subject with a female partner of child bearing potential who does not agree to use effective contraception during the study and for 3 months after the last dose of ODM 203
Known hypersensitivity to the study treatment excipients
Any condition which in the opinion of the investigator would impair the subject's ability to comply with the study procedures
Participation in another interventional clinical trial/ concurrent treatment with any investigational drug within 4 weeks prior to the start of treatment with ODM 203