Thrombolysis With Recombinant Non-immunogenic Staphylokinase vs Surgery in Patients With Acute Limb Ischemia FORAT Trial

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorSupergene, LLC

About this trial

Objective: to evaluate the efficacy and safety of intra-arterial intrathrombus administration of the recombinant non-immunogenic staphylokinase (Fortelyzin®) in patients with acute limb ischemia (ALI) vs surgery.

Eligibility criteria

Qualifiers

Men and women aged 18 and older;

Diagnosis of I-II b degree of ALI;

women who have a negative pregnancy test and use the following contraceptives: intrauterine devices, oral contraceptives, contraceptive patch, prolonged injectable contraceptives, double barrier method of contraception. Women who are not fertile can also take part in the study (documented conditions: hysterectomy, tubal ligation, infertility, menopause for more than 1 year);

men using barrier contraception. The study may also involve men who are not fertile (documented conditions: vasectomy, infertility);

Disqualifiers

Extensive bleeding at present;

Intracranial (including subarachnoid) hemorrhage at present;

Recent gastrointestinal bleeding (within 10 days);

Major surgery or major trauma within the previous 3 months, recent traumatic brain injury;

Trial design

Treatments tested in this trial

  • Recombinant non-immunogenic staphylokinase (Fortelyzin®)
  • surgical methods of treatment

Treatment groups

170 Participants
are divided into 2 treatment groups

Sponsors and collaborators