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Dose-finding Study of BP-C1 in Patients With Stage IV Breast Cancer

Phase 1
Completed
Conditions
Metastatic Breast Cancer
Stage IV Breast Cancer
Interventions
Registration Number
NCT04298333
Lead Sponsor
Meabco A/S
Brief Summary

The purpose of this study is to estimate the cumulative Maximum Tolerated Dose (MTD) and Minimum Efficient Dose (MED) of BP-C1 in the short-term treatment of metastatic breast cancer patients.

Detailed Description

BP-C1, solution for injection 0.05%, is currently being developed for treatment of patients with metastatic breast cancer with palliative intent. Active substance of the product, which is a novel platinum-containing anticancer agent developed for intramuscular administration, is a cis-diammineplatinum(II) complexed with a polymer containing benzene polycarboxylic acids derived from lignin. The amphiphilic characteristics of the polymer have resulted in a product with clear and significantly altered and improved properties compared to other platinum analogues, e.g. cisplatin, carboplatin and oxaliplatin.

BP-C1 preserves antitumour activity of its predecessors (e.g. cisplatin and carboplatin), additionally offering the following advantages that ensure favourable outcome of treatment of metastatic breast cancer patients:

* injectable solution (intramuscular) does not cause injection site reactions;

* can be administered at home by a nurse or a patient;

* has an improved pharmacokinetic profile;

* demonstrates efficacy comparable to cisplatin and much higher than carboplatin (in-vitro; in-vivo data);

* exerts an additional immunomodulatory activity.

In this study BP-C1 will be administered as supportive care to patients with metastatic breast cancer (stage IV), who had undergone at least three lines of chemotherapy.

This study will be open-label, multi-centre with a sequential safety design based on 3-level between-patient Response Surface Pathway (RSP) algorithm. The eligible patients will be allocated to five independent sequences, with three patients in each sequence. The BP-C1 treatment period will be 32 days, the follow-up period will be 28 days after the last BP-C1 dose.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
18
Inclusion Criteria

Female patients with histologically verified metastatic breast cancer (stage IV) with measurable metastases, between 18 and 80 years of age, who had undergone at least three lines of chemotherapy and had an expected survival time of at least 3 months.

Exclusion Criteria

Patients fulfilling at least one of the following criteria will be excluded from participation in the study:

  • Abnormal liver function classified as total bilirubin >34 μmol/L or ALAT > 3 times of the upper limit of normal (ULN). In case of metastases in the liver, the ALAT limit for exclusion is set to 5хULN.
  • Abnormal kidney function defined by serum creatinine >120 μmol/L.
  • Abnormal coagulation capacity defined by the relative arbitrary concentration of coagulation factors 2,7,10; INR >1.5.
  • Verified metastases to the brain.
  • Synchronous cancer except for non-melanoma skin cancer and early stage of cervical cancer.
  • Abnormal haematology status defined by haemoglobin < 9.0 g/dL, platelet count < 100,000/mm^3 or leucocytes < 3x10^9/L.
  • Clinically significant abnormal ECG.
  • Karnofsky performance status score <60%.
  • Pregnant or breast feeding women.
  • Women of fertile age who do not want to be tested for possible pregnancy.
  • Fertile female who do not want to use safe protection against pregnancy, starting one month before the start of the study treatment and lasting at least six weeks after.
  • Uncontrolled bacterial, viral, fungal or parasite infection.
  • Under systemic treatment with corticosteroids or other immunosuppressive drugs in the last 21 days before start of the trial treatment.
  • Participating in another clinical trial with pharmaceuticals in the last six weeks before start of this trial treatment.
  • Not able to understand information.
  • Not willing or not able to give written consent to participate in the study.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
BP-C1BP-C1BP-C1 will be used as supportive care
Primary Outcome Measures
NameTimeMethod
Change in Maximum Common Terminology Criteria (CTC) score for Adverse Eventsbaseline to Day 32 of treatment and Day 28 of follow-up

Maximum CTC score will be recorded using CTC v2.0 given as the highest observed CTC score at a given visit. The CTC scores will be recorded using CTC v2.0 divided in 15 System Organ Classes

Sum Common Terminology Criteria (CTC) score for Adverse Eventsbaseline to Day 32 of treatment and Day 28 of follow-up

The Sum CTC score will be a sum of all registered CTC scores obtained at a given visit. The CTC scores will be recorded using CTC v2.0 divided in 15 System Organ Classes

Secondary Outcome Measures
NameTimeMethod
Proportion of patients with Disease Control Rate (DCR)baseline to Day 32 of treatment and Day 28 of follow-up

The DCR defined as patients classified as SD, PR, CR

Treatment Responsebaseline to Day 32 of treatment and Day 28 of follow-up

In accordance with RECIST v1.1 the treatment response will be classified as 'complete response', 'partial response', 'stable disease' or 'progressive disease': Complete response (CR): disappearance of all target lesions. Partial response (PR): at least 30% decrease in the sum of longest diameters of target lesions, taking as reference the baseline sum of diameters. Progressive disease (PD): at least 20% increase in the sum of diameters of target lesions.

Number of registered Adverse Events (AEs)baseline to Day 32 of treatment period and Day 28 of follow-up

Trial Locations

Locations (3)

Siriraj Hospital, Mahidol University

🇹🇭

Bangkok, Thailand

National Taiwan University Hospital

🇨🇳

Taipei, Taiwan

Sanglah University Hospital

🇮🇩

Bali, Indonesia

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