ClinicalTrials.gg
RecruitingNCT07108309AREALUpdated Aug 7, 2025

BCD-236 in Combination With Chemotherapy in Patients With Relapsed and/or Metastatic Triple Negative Breast Cancer

A Phase 2 interventional study of BCD-236 and Chemotherapy in Triple Negative Breast Cancer, sponsored by Biocad. Recruiting at 47 sites in 2 countries. Open to female participants aged 18 Years to 74 Years. Per ClinicalTrials.gov, last updated 2025-08-07.

Sponsored by Biocad · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Dec 2025, 11 months ago, but the record still lists the study as recruiting.
  • Registered 1 year after the study started (first participant enrolled Jul 2024, registered Aug 2025).
  • Started Jul 2024; still recruiting 2 years 3 months later.
Phase
Phase 2
Study type
Interventional
Enrollment
124
Allocation
Randomized
Ages
18 Years to 74 Years
Sex
Female
01

Study summary

To study the efficacy, safety, pharmacokinetics and immunogenicity of BCD-236 in combination with chemotherapeutic agents (CHT) in 2nd and subsequent lines of therapy of subjects with relapsed and/or metastatic triple negative breast cancer (TNBC).

02

Conditions studied

  • Triple Negative Breast Cancer
03

In context

Triple Negative Breast Neoplasms

1,219 studies on the registry are indexed under Triple Negative Breast Neoplasms; 446 are open to participants now.

This study's planned enrollment of 124 is above the median of 60 across 1,053 interventional studies indexed under Triple Negative Breast Neoplasms.

Browse Triple Negative Breast Neoplasms studies →

Lead sponsor

Biocad is the lead sponsor of 94 studies on the registry; 12 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 74 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Eligibility criteria

Main Inclusion Criteria:

  • Signed and the subject's ability to comply with the requirements of the Clinical Study Protocol.
  • Age ≥18 years and \<75 years at the time of signing the informed consent form.
  • verified diagnosis (there are documented results of relevant studies) of TNBC: ER 0-2 points, PR 0-2 points or ER \<1%, PR \<1% (ASCO/CAP); (≤1+) or HER2 (2+) in the absence of amplification of the Her-2-neu gene by ISH.
  • TNBC is progressive or relapsing on or after systemic therapy.
  • The subject received at least 1 for locally advanced unresectable or TNBC, or she experienced a relapse / progressive disease during or within 6 months after completion of post-operative (adjuvant) chemotherapy.
  • Confirmed AXL expression in tumor cells according to immunohistochemistry.
  • Availability of fresh (obtained as part of screening or before its start, but after disease progression or relapse on the last line of therapy) and archival (obtained before disease progression or relapse on the last line of therapy, if available) tumor material samples suitable for immunohistochemical examination to determine AXL expression.
  • Presence of at least 1 measurable tumor lesion according to 1.1. criteria for CIR.
  • score 0-1.
  • ≥ 4 months from the date of signing of the informed consent form in the opinion of the Investigator.

Main Exclusion Criteria:

  • Indications for radical therapy or radiotherapy (excluding minor surgery or radiation therapy for palliative purposes).
  • Active and/or carcinomatous meningitis. Subjects with brain metastases may participate in the study provided that the metastases have been adequately treated with surgery or radiotherapy, and if they have been clinically stable for at least 4 weeks prior to randomization (i.e. no neurological symptoms, no need for , and no lesions >1.5 cm) and no evidence of new or increasing CNS metastases. Patients with newly diagnosed CNS metastases during screening may not be included in the study.
Terms in these criteria, in plain language(10)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Histologically or cytologically confirmed

The diagnosis was confirmed by looking at a sample under a microscope: tissue from a biopsy or surgery (histology), or cells from a fluid or needle sample (cytology).

Your pathology report is the document that shows this.

HER2

HER2 is a protein, made from the ERBB2 gene, that drives the growth of some cancers. A study may look for a level of the protein, extra copies of the gene, or a particular change in it.

In breast cancer, protein tests are read as HER2-positive, HER2-low or HER2-negative; other cancers use their own rules. Check which test result the study requires.

Line of therapy

A line of therapy is one course of treatment, which may combine several drugs. First-line is the first course given; second-line follows when that stops working or is not tolerated.

“Two prior lines” means two courses that count separately under the study’s rules — not simply two drugs. Ask the study team if you are unsure how yours are counted.

Metastases

Cancer that has spread from where it began to other parts of the body. “Metastatic” cancer is cancer that has spread this way.

RECIST

The standard rules for measuring tumours on CT or MRI scans, to tell whether a cancer is shrinking, stable or growing during treatment.

“Measurable disease per RECIST 1.1” usually means at least one tumour 10 mm or more at its longest on a CT scan, or a lymph node 15 mm or more across its short axis.

ECOG performance status

A scale of how much an illness limits everyday activity. For people being assessed to join a study, scores run from 0 (fully active) to 4; lower is more active.

0
Fully active, no restrictions.
1
Limited in strenuous activity, but walking and able to do light work, such as housework or office work.
2
Walking and able to look after yourself, but unable to work; up and about more than half of waking hours.
3
Able to look after yourself only in part; in bed or a chair more than half of waking hours.
4
Unable to look after yourself at all; in bed or a chair all day.

Studies most often ask for 0–1 or 0–2. Your doctor gives the score; the WHO scale uses the same steps. The full scale also has 5, which records death.

Life expectancy

The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.

Brain metastases

Cancer deposits in the brain from a cancer that started elsewhere in the body (CNS metastases include the spinal cord).

Studies differ: some leave out any brain metastases, some accept ones treated and stable for some weeks. Check what this study allows.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
124 participants (estimated)

Study arms

  • Experimental
    BCD-236 + Chemotherapy (CHT)

    Subjects will receive BCD-236 +CHT Duration of treatment: until disease progression or intolerable toxicity or EOS

    Biological: BCD-236 · Drug: Chemotherapy

  • Active comparator
    Chemotherapy (CHT)

    Subjects will receive CHT. Duration of treatment: until disease progression or intolerable toxicity or EOS

    Drug: Chemotherapy

Interventions

  • BiologicalBCD-236

    as an intravenous infusion

  • DrugChemotherapy

    CHT (at the investigator's discretion):

06

What researchers measure

Primary outcomes

  1. Overall response rate (ORR)

    According to RECIST 1.1 criteria by the central independent review (CIR)

    Time frame: 24 weeks

Secondary outcomes

  1. Progression-free survival (PFS)

    According to RECIST 1.1 criteria by the central independent review (CIR)

    Time frame: 51 and 102 weeks

  2. Overall survival (OS)

    Time frame: 102 weeks

  3. Disease control rate (DCR)

    According to RECIST 1.1 criteria by the central independent review (CIR)

    Time frame: 24 weeks

  4. Time to response

    According to RECIST 1.1 criteria by the central independent review (CIR)

    Time frame: 24 weeks

  5. Duration of response

    According to RECIST 1.1 criteria by the central independent review (CIR)

    Time frame: 24 weeks

07

Study locations

40 of 47 sites recruiting
  • Health Institution "Brest Regional Oncology Center"
    Brest, Belarus
    Recruiting
  • "Gomel Regional Clinical Oncology Dispensary"
    Homyel, Belarus
    Recruiting
    • Vasily N Belyakovsky · Contactmail@gokod.by · +375 232 20 76 00
  • Minsk City Oncology Center
    Minsk, Belarus
    Recruiting
    • Svetlana A Demidova · Contactonko@mgkoc.by · +375 17 355 61 97
  • State Budgetary Institution of Healthcare of the Arkhangelsk Region "Arkhangelsk Clinical Oncology Dispensary"
    Arkhangelsk, Russia
    Active, not recruiting

    Not enrolling at this site — choose another above.

  • Regional State Budgetary Healthcare Institution "Altai Regional Oncology Dispensary"
    Barnaul, Russia
    Active, not recruiting

    Not enrolling at this site — choose another above.

  • SBHI "Chelyabinsk regional clinical center Oncology and nuclear medicines"
    Chelyabinsk, Russia
    Recruiting
    • Natalya V Fadeeva · Contact
  • Budgetary healthcare institution of the Udmurt Republic "Republican clinical oncology dispensary named after Sergei Grigorievich Primushko of the Ministry of Health of the Udmurt Republic
    Izhevsk, Russia
    Recruiting
    • Sergey A Emelyanov · Contact+7 (3412) 50 88 00
  • SBHI of the Kaluga Region "Kaluga Regional Clinical Oncology Center"
    Kaluga, Russia
    Recruiting
  • State Autonomous Institution of Health "Republican Clinical Oncological Dispensary of the Ministry of Health of the Republic of Tatarstan named after prof. M.Z.Sigal"
    Kazan', Russia
    Recruiting
  • SBHI "Clinical oncological Dispensary № 1" of the Ministry of Health of the Krasnodar Territory
    Krasnodar, Russia
    Recruiting
    • Alexey A Leonov · Contactkkod@kkod.ru · +7 (861) 233 66 04
  • Branch of company "Hadassah Medical LCC"
    Moscow, Russia
    Recruiting
  • Federal State Budgetary Scientific Institution "Russian Scientific Center of Surgery named after Academician B.V. Petrovsky"
    Moscow, Russia
    Recruiting
    • Lyubov V Krivolapova · Contactinfo@med.ru · +7 (499) 248 15 55
  • FSAEI of Higher Education "First Moscow State Medical University named after I.M. Sechenov" of the Ministry of Health of the Russian Federation
    Moscow, Russia
    Recruiting
  • FSAEI of Higher Education I.M. Sechenov First Moscow State Medical University of the Ministry of Health of the Russian Federation (Sechenov University)
    Moscow, Russia
    Recruiting
  • FSAI "National Medical Research Center for Therapeutic and Rehabilitation Center" of the Ministry of Health of the Russian Federation
    Moscow, Russia
    Recruiting
  • FSBI "Lopukhin Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency"
    Moscow, Russia
    Recruiting
  • FSBI "National Medical Research Center of Oncology named after N. N. Blokhin" of the Ministry of Health of the Russian Federation
    Moscow, Russia
    Recruiting
    • Elena V Artamonova · Contactinfo@ronc.ru · +7 (499) 444 24 24
  • Joint Stock Company "Medsi Group of Companies"
    Moscow, Russia
    Recruiting
    • Anastasia S Mochalova · Contact+7 (495) 152 47 53
  • JSC "Modern medical technologies"
    Moscow, Russia
    Recruiting
  • Limited Liability Company "Moscow Center for Rehabilitation Treatment"
    Moscow, Russia
    Recruiting
  • SBHI of the City of Moscow "Moscow Clinical Scientific and Practical Center named after A.S. Loginov of the Moscow City Health Department"
    Moscow, Russia
    Recruiting
    • Lyudmila G Zhukova · Contactinfo@mknc.ru · +7 (495) 304 30 39
  • State Budgetary Institution of Healthcare of the City of Moscow "City Clinical Hospital named after S.S. Yudin of the Moscow City Health Department
    Moscow, Russia
    Recruiting
  • State Budgetary Institution of Healthcare of the City of Moscow "Moscow City Oncology Hospital No. 62 of the Moscow City Healthcare Department"
    Moscow, Russia
    Recruiting
  • SAHI of the Nizhny Novgorod region "Research Institute of Clinical Oncology "Nizhny Novgorod Regional Clinical Oncological Dispensary"
    Nizhny Novgorod, Russia
    Recruiting
  • FBHI of the Novosibirsk Region "Novosibirsk Regional Clinical Oncological Dispensary"
    Novosibirsk, Russia
    Recruiting
    • Vadim V Kozlov · Contactnood@nso.ru · +7 (383) 382 80 46
  • FSBI "National Medical Research Center for Radiology" of the Ministry of Health of the Russian Federation
    Obninsk, Russia
    Recruiting
  • FSBI "National Medical Research Center of Radiology" of the Ministry of Health of the Russian Federation Medical Radiological Research Center named after A.F. Tsyb
    Obninsk, Russia
    Active, not recruiting

    Not enrolling at this site — choose another above.

  • Budget Healthcare Institution of the Omsk region "Clinical Oncological Dispensary"
    Omsk, Russia
    Recruiting
  • FSBI "National Medical Research Center of Oncology" of the Ministry of Health of the Russian Federation
    Rostov-on-Don, Russia
    Recruiting
  • State budgetary institution of the Ryazan region "Regional clinical oncology dispensary"
    Ryazan, Russia
    Recruiting
  • FSBEI of Higher Education "North-Western State Medical University named after I. I. Mechnikov" of the Ministry of Health of the Russian Federation
    Saint Petersburg, Russia
    Recruiting
  • FSBI "National medical research center of Oncology named after N.N. Petrov" Of Ministry of Health of the Russian Federation, Department of Breast Cancer Surgery
    Saint Petersburg, Russia
    Recruiting
  • FSBI "National medical research center of Oncology named after N.N. Petrov" Of Ministry of Health of the Russian Federation, Research Division of Innovative Techniques in Medical Oncology and Rehabilitation Medicine
    Saint Petersburg, Russia
    Recruiting
  • LLC "NRC Eco-Safety"
    Saint Petersburg, Russia
    Recruiting
  • LLC "VitaMed"
    Saint Petersburg, Russia
    Recruiting
  • Private healthcare institution "Clinical hospital "RZD-Medicine" of the city of St. Petersburg"
    Saint Petersburg, Russia
    Recruiting
    • Alexander G Vasiliev · Contact+7 (812) 62 29 762
  • Private medical institution "Euromedservice"
    Saint Petersburg, Russia
    Recruiting
  • SBHI "St. Petersburg Clinical Scientific and Practical Center for Specialized Types of Medical Care (Oncological) named after N.P. Napalkov"
    Saint Petersburg, Russia
    Recruiting
  • SBHI of St. Petersburg "City Clinical Oncology Dispensary"
    Saint Petersburg, Russia
    Recruiting
  • State Budgetary Healthcare Institution Leningrad Regional Clinical Hospital
    Saint Petersburg, Russia
    Active, not recruiting

    Not enrolling at this site — choose another above.

  • Federal State Budgetary Educational Institution of Higher Education "National Research Mordovian State University named after N.P. Ogarev"
    Saransk, Russia
    Recruiting
    • Pavel I Skopin · Contactmrsu@mrsu.ru · +7 (8342) 24 37 32
  • SBHI Arkhangelsk Region "Severodvinsk City Clinical Hospital No. 2 for Emergency Medicine"
    Severodvinsk, Russia
    Recruiting
  • State Budgetary Healthcare Institution "Tambov Regional Oncology Clinical Dispensary"
    Tambov, Russia
    Active, not recruiting

    Not enrolling at this site — choose another above.

  • SAHI Republican Clinical Oncology Dispensary of the Ministry of Health of the Republic of Bashkortostan
    Ufa, Russia
    Recruiting
  • SBHI "Volgograd Regional Clinical Oncological Dispensary"
    Volgograd, Russia
    Active, not recruiting

    Not enrolling at this site — choose another above.

  • SBHI of the Yaroslavl region "Regional Clinical Oncological Hospital"
    Yaroslavl, Russia
    Recruiting
  • SAHI of the Sverdlovsk region "Sverdlovsk Regional Oncological Center"
    Yekaterinburg, Russia
    Active, not recruiting

    Not enrolling at this site — choose another above.

08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jul 2024 (actual). Primary completion is estimated for Dec 2025, 17 months after the start.

Of 255 phase 2 interventional studies under Triple Negative Breast Neoplasms, half reached primary completion within 59 months of starting (the median), counting those still running; a quarter within 37 and three quarters within 94. This study's planned 17 months is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 4, 2025
First posted
Aug 7, 2025
StartActual
Jul 15, 2024
Primary completionEst.
Dec 2025
CompletionEst.
May 2027
Last update
Aug 7, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 7, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07108309
Lead sponsor
Biocad
Responsible party
Sponsor
First posted
Aug 7, 2025
Start date
Jul 15, 2024
Primary completion
Dec 2025 (estimated)
Completion
May 2027 (estimated)
Last update
Aug 7, 2025

Study contacts

Evgenia А Mikhailova
Contact
mikhailova@biocad.ru
+7 911 081 23 68
Arina V Zinkina-Orikhan, PhD
study director · Director of Clinical Development Department, BIOCAD

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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