Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster display session: Breast cancer - early stage, locally advanced & metastatic, CNS tumours, Developmental therapeutics, Genitourinary tumours - prostate & non-prostate, Palliative care, Psycho-oncology, Public health policy, Sarcoma, Supportive care

3354 - Safe switch of treatment from the reference product to RGB-02, a proposed biosimilar pegfilgrastim: analysis of the results of three clinical trials

Date

22 Oct 2018

Session

Poster display session: Breast cancer - early stage, locally advanced & metastatic, CNS tumours, Developmental therapeutics, Genitourinary tumours - prostate & non-prostate, Palliative care, Psycho-oncology, Public health policy, Sarcoma, Supportive care

Topics

Supportive Care and Symptom Management

Tumour Site

Presenters

Andras Illes

Citation

Annals of Oncology (2018) 29 (suppl_8): viii603-viii640. 10.1093/annonc/mdy300

Authors

A. Illes1, L. Perjesi1, K. Horvat-Karajz2, N. Jeszenoi1, I. Aradi2, N.K. Singh3, S.J. Mair3, Z. Kahan4

Author affiliations

  • 1 Clinical Development Of Biologics, Gedeon Richter Plc., 1103 - Budapest/HU
  • 2 Clinical Development Of Biologics, Gedeon Richter Plc., Budapest/HU
  • 3 Medical Department, Quotient Sciences, Ruddington/GB
  • 4 Dept. Oncotherapy, University of Szeged, 6720 - Szeged/HU

Resources

Login to access the resources on OncologyPRO.

If you do not have an ESMO account, please create one for free.

Abstract 3354

Background

Treatment with recombinant human granulocyte-colony stimulating factor (G-CSF) is an accepted standard for prevention of chemotherapy-induced neutropenia. RGB-02, a pegylated G-CSF (pegfilgrastim) developed by Gedeon Richter is a proposed biosimilar to the reference product Neulasta®. Therapy switch from a reference product to its biosimilar is expected to occur in the daily practice. Here we are presenting the outcome of treatment switch in two randomized cross-over design comparative PK/PD studies (EudraCT nr: 2011-001737-17 and 2016-005051-25) and a randomized, comparative, multicenter efficacy and safety study of RGB-02 (EudraCT nr: 2013-003166-14).

Methods

Efficacy, safety and PD data of two PK/PD studies (enrolling 110 and 150 healthy volunteers, respectively) and a comparative efficacy and safety study (enrolling 239 breast cancer patients) were analyzed in order to assess whether treatment switch from Neulasta® to RGB-02 has any impact on the PD response, efficacy or safety. The PK/PD studies had a cross-over design. Patients in the reference arm of the comparative efficacy and safety study were switched to RGB-02 treatment following the first two chemotherapy cycles. Endpoints assessed were related to the change in ANC count in healthy volunteers, duration of severe neutropenia (DSN; ANC < 0.5 x109/L) in the comparative efficacy and safety study, as well as safety data including immunogenicity collected in each clinical study.

Results

None of the PD endpoints showed any difference following the cross-over in the comparative PK/PD studies. The mean DSN values after the therapy switch were similar to the values prior to the switch and the switched arm (mean DSN: 0.6) did not show decreased efficacy compared to the arm received RGB-02 from the first cycle (mean DSN: 0.9). Safety results, including immunogenicity of the 3 studies did not reveal any negative impact of the treatment switch.

Conclusions

Treatment switch from Neulasta® to RGB-02 can be considered safe while maintaining the therapeutic effect of pegfilgrastim therapy.

Clinical trial identification

EudraCT: 2011-001737-17; EudraCT: 2016-005051-25; EudraCT: 2013-003166-14.

Legal entity responsible for the study

Gedeon Richter Plc.

Funding

Gedeon Richter Plc.

Editorial Acknowledgement

Disclosure

A. Illes L. Perjesi, K. Horvat-Karajz, N. Jeszenoi, I. Aradi: Employee: Gedeon Richter Plc. N.K. Singh, S.J. Mair, Z. Kahan: Principal investigator of one of the studies (EudraCT Nr. 2016-005051-25) sponsored by Gedeon Richter Plc; Investigator grant from the sponsor.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.