Completed Cancer NIHR-supported project Lungs & Breathing

CCS1477-02: An open-label Phase I/IIa study to evaluate the safety and efficacy of CCS1477 as monotherapy and in combination in patients with advanced haematological malignancies (Multiple Myeloma arm)

In plain English

AI plain-English summary

A new experimental drug called CCS1477 is being tested in around 90 UK patients whose blood cancers—including multiple myeloma, acute myeloid leukaemia, and non-Hodgkin lymphoma—have stopped responding to existing treatments. This matters because advanced haematological malignancies often become resistant to standard therapies, leaving patients with few options. The drug targets a protein involved in cancer cell growth, and the trial will assess its safety, how the body processes it, and whether it shrinks tumours or slows disease progression. The study runs across up to 10 UK hospitals and includes dose escalation and expansion phases. If CCS1477 proves safe and effective, it could become a new treatment option for patients with relapsed or refractory blood cancers—conditions where current drugs frequently fail. The results will determine whether the drug moves into larger, later-stage trials. For now, the research is an early-stage clinical test: it will not change practice immediately, but it provides the essential safety and efficacy data needed to decide whether CCS1477 is worth pursuing further.

View original technical description
CCS1477 is a new experimental medication (sponsored by CellCentric Ltd) for a group of cancers that effect the blood and/or bone marrow. These include Acute Myeloid Leukaemia (AML), high-risk Myelodysplastic Syndrome (MDS), Multiple Myeloma (MM) and Non-Hodgkin Lymphoma (NHL). It is aimed at tumours that are not responsive to, or have become resistant to, existing medications used in late stage disease.The purpose of this study is to examine the safety, tolerability, pharmacokinetics (PK) and efficacy of CCS1477 when treating patients with the above disorders. It is expected that approximately 90 patients will be recruited from up to 10 hospitals in the UK. The study has 5 parts consisting of dose escalation and expansion cohorts. Patients will have regular clinic visits for various safety and clinical benefit assessments, to monitor any side effects and to find out how CCS1477 is handled by the body and affects this group of cancers.The information gained in this study will help the sponsor to determine whether CCS1477 is suitable for further studies in humans.

Researchers

Sally Moore (Principal Investigator)

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CCS1477-02 - An open-label Phase I/IIa study to evaluate the safety and efficacy of CCS1477 as monotherapy in patients with advanced haematological malignancies
An open-label Phase I/IIa study to evaluate the safety and efficacy of CCS1477 as monotherapy in patients with advanced haematological malignancies.
An open-label Phase I/IIa study to evaluate the safety and efficacy of CCS1477 as monotherapy and in combination, in patients with advanced solid/metastatic tumours.
An open-lab el Phase I/IIa study to evaluate the safety and efficacy of CCS1477 as monotherapy in patients with advanced haematological malignancies
An open-label Phase I/IIa study to evaluate the safety and efficacy of CCS1477 as monotherapy in patients with advanced haematological malignancies

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