A Study to Assess a New Medicine Called IPN01195 When Administered Alone in Adults With Advanced Solid Tumours

Trial statusRecruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorIpsen

About this trial

The purpose of this study is to determine the appropriate dosage, safety and effectiveness of a new study drug IPN01195 in adults with advanced solid tumours.

The participants in this study will have advanced solid tumours. 'Advanced solid tumours' refers to cancers that can occur in several places, including cancers in organs or tissues that have spread from their original site to nearby tissues or other parts of the body.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Participants must be ≥18 years of age or the country's legal age of majority if the legal age is more than 18 years at the time of signing the informed consent.

Participants with histologically confirmed metastatic solid tumour for whom no suitable alternative standard therapy exists.

Participants must bear tumours harbouring selected classes of genetic alterations of MAPK pathway based on an analytically validated assay performed by an accredited laboratory.

Part A: Participants must consent to the use of archival tumour tissue or, if not available, collection of fresh tumour biopsy at screening, for central confirmation of mutation status.

Disqualifiers

Gastrointestinal conditions that could impair absorption of IPN01195 (specific cases e.g. remote history of gastrointestinal surgery, may be enrolled after discussion with the medical monitor)

Any evidence of severe active infection or inflammatory condition.

Non-adequate cardiac function

Known psychiatric or substance abuse disorder, or any other cognitive disorder per the opinion of the investigator that would interfere with the participant's ability to cooperate with the requirements of the study.

Trial design

Design model

Sequential

Treatments tested in this trial

  • IPN01195

    Drug

    IPN01195 will be administered at assigned dose level.

Treatment groups

85 Participants
are divided into 2 treatment groups
Group A: Part A (dose escalation)Experimental treatment 1 intervention
Group B: Part B - (randomisation)Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Part A: Percentage of participants with dose limiting toxicity (DLT)

Time frame
Part A: within 28 days of first dose.
2

Part A and B: Percentage of participants experiencing treatment emergent adverse events (TEAEs) and treatment emergent serious adverse events (TE SAEs).

An Adverse event (AE) is any untoward medical occurrence in a clinical study participant, temporally associated with the use of study intervention, whether or not considered related to the study intervention. TEAE is an AE for which the start date is on or after the date that the intervention began.

Time frame
From the first IPN01195 administration to 30 days after last dose.
3

Part A and B: Percentage of participants with dose interruptions and permanent treatment discontinuations

Time frame
From the first study drug administration to 30 days after last dose.
4

Part B: Objective response rate (ORR)

Objective response rate is defined as the percentage of participants with best overall response (BOR) of complete response (CR) or partial response (PR) as determined by investigator per RECIST version 1.1.

Time frame
Part B: At end of study (up to approximately 3 years)

Secondary outcomes

1

Part A: Time to maximum observed drug concentration (Tmax) after single and multiple doses of IPN01195

Time frame
Cycle 1: at Day 1 and at Day 15.
2

Part A: Maximum observed drug concentration (Cmax) after single and multiple doses of IPN01195

Time frame
Cycle 1: at Day 1 and at Day 15.
3

Part A: Area under the plasma concentration time curve (AUCtau) after single and multiple doses of IPN01195

AUCtau is defined as the concentration of drug over one dosing interval.

Time frame
Cycle 1: at Day 1 and at Day 15.
4

Part A: Geometric mean ratio of Cmax of IPN01195 administered in fed state relative to fasted state.

Time frame
Between Day -8 and Day -3 (fasted period) and between Day -10 and Day -7 (fed state period)

Other outcomes

Sponsors and contacts

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