Tinzaparin And Biomarkers After Neoadjuvant Treatment of Ovarian Cancer

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexFemale
Age18+
SponsorUniversity Hospital, Linkoeping

About this trial

Background:

Previous findings have indicated antineoplastic properties of tinzaparin (Innohep®), a commonly used anti-coagulant. Earlier studies have mainly investigated the antineoplastic effects of tinzaparin in animal models and in human cell-lines. In this pilot study the aim is to examine the potential antitumoral effects of tinzaparin in vivo in women with epithelial ovarian cancer (EOC).

Study objectives:

Primary objective: The primary objective of the study is to evaluate the effects of tinzaparin on changes in levels of CA-125 in EOC patients who receive neoadjuvant chemotherapy (NACT).

Secondary objectives: The secondary objective of the study is to explore the impact of tinzaparin on the dynamic of a spectrum of immunological and coagulation factors in EOC patients who receive NACT. Besides, the compliance of tinzaparin injections and adverse events caused by tinzaparin will be described.

Eligibility criteria

Qualifiers

The subject has given written consent to participate in the study.

Age 18 and above

Epithelial ovarian, fallopian tube or peritoneal cancer, or abdominal cancer where a biopsy indicates an origin from the ovary, fallopian tube or peritoneum.

Histology diagnosis of either high grade serous carcinoma, endometroid carcinoma or clear cell carcinoma.

Disqualifiers

Concomitant treatment with heparins, low molecular weight heparins, warfarin or non-vitamin K antagonist oral anticoagulants. Platelet inhibitors are allowed.

Treatment with heparins, low molecular weight heparins or non-vitamin K antagonist oral anticoagulants within the last year.

Known or suspected allergies against any product included in the study

Ongoing pregnancy, independent of gestational age. Breastfeeding or planned pregnancy

Trial design

Treatments tested in this trial

  • Tinzaparin Injectable Solution

Treatment groups

40 Participants
are divided into 2 treatment groups

Sponsors and collaborators

University Hospital, Linkoeping

Lead sponsor

Region Jönköping County

Collaborator

Västervik Hospital

Collaborator

Vastra Gotaland Region

Collaborator

Region Västerbotten

Collaborator