ClinicalTrials.gg
RecruitingNCT06668792FLAMMINGOUpdated Feb 4, 2025

An Open-Label Clinical Study of the Efficacy and Safety of BCD-248 in Patients with Relapsed/Refractory Multiple Myeloma

A Phase 2 interventional study of BCD-248 in Relapsed/Refractory Multiple Myeloma, sponsored by Biocad. Recruiting at 20 sites in Russian Federation. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-02-04.

Sponsored by Biocad · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Feb 2026, 9 months ago, but the record still lists the study as recruiting.
  • Started Dec 2024; still recruiting 1 year 10 months later.
Phase
Phase 2
Study type
Interventional
Enrollment
100
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

The aim of the study is to assess the efficacy and safety of BCD-248 as a therapy for relapsing and/or refractory multiple myeloma.

02

Conditions studied

  • Relapsed/Refractory Multiple Myeloma

Browse trials for

03

In context

Multiple Myeloma

3,760 studies on the registry are indexed under Multiple Myeloma; 769 are open to participants now.

This study's planned enrollment of 100 is above the median of 41 across 3,005 interventional studies indexed under Multiple Myeloma.

Browse Multiple Myeloma 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 and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Signed form.
  2. Age ≥18 years.
  3. Documented diagnosis of multiple myeloma according to the IMWG criteria.
  4. at screening.
  5. Subjects who received at least 2 for multiple myeloma, including a proteasome inhibitor, an immunomodulatory drug, anti-CD38 therapy.
  6. Documented progression according to the IMWG criteria during or after the last line of therapy.
  7. Evidence of at least a partial response according to the IMWG criteria to at least 1 previous line of therapy.
  8. score 0-2.

Exclusion criteria

Exclusion Criteria:

  1. Subjects who were previously treated with anti-BCMA or anti-CD3 drugs.
  2. Use of any medicinal products or medical devices within 30 days or 5 half-lives (whichever is longer) prior to the expected start of the study therapy or planned use of investigational medicinal products or medical devices during participation in this study, except for the use described in this Protocol.
  3. hematopoietic stem cell transplantation within 12 weeks prior to the expected start of the study therapy or a history of allogenic stem cell transplantation, regardless of when it was performed.
  4. Planned hematopoietic stem cell transplantation before disease progression during this study.
  5. A history of other within 5 years before screening, excluding squamous and basal cell skin cancers, carcinoma in situ of the cervix or breast, or other malignancies, which, in the opinion of the Investigator, have been adequately treated and have a minimal risk of recurrence within 5 years.
  6. Concomitant diseases and/or conditions that significantly increase the risk of AEs during the study:

    • Stable angina pectoris, functional class III-IV.
    • Unstable angina and/or myocardial infarction within less than 6 months before the expected start of the study therapy.
    • Chronic heart failure, class III-IV;
    • (in the Investigator's opinion) cardiac arrhythmia and conduction disorders that do not respond to the maximum possible antiarrhythmic therapy (therapy should be stable for 4 weeks before the expected start of the study therapy);
    • Moderate to severe asthma, grade III-IV , a history of angioedema, severe respiratory failure;
    • Active diseases (subjects with type 1 diabetes mellitus and hypothyroidism requiring only hormone replacement therapy, as well as with skin diseases (vitiligo, alopecia, or psoriasis) that do not require systemic therapy are eligible);
    • Any infection within 14 days prior to the expected start of the study therapy, requiring systemic etiotropic therapy or which, in the opinion of the Investigator, may increase the risk of infectious complications;
    • Any other concomitant disease or condition, which, in the Investigator's opinion, significantly increases the risk of AEs in the study.
  7. Subjects with amyloidosis.
  8. Clinical signs of meningeal involvement of multiple myeloma.
  9. infection, active infection, .
  10. Major surgery within less than 14 days prior to the expected start of the study therapy, incomplete recovery from surgery, or planned surgery during participation in the study.
  11. Pregnancy or breastfeeding, as well as intention to become pregnant or father a child during the study period and within 180 days after receiving the last dose of the IP.
Terms in these criteria, in plain language(14)

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.

Measurable disease

The amount of disease can be tracked with a defined measurement, so the study can see whether it shrinks or grows. It might be a tumour measured on a scan or, in some blood cancers such as myeloma, a marker measured in blood or urine.

The criteria or the study team say which measurement counts — having no tumour visible on a scan does not by itself rule you out.

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.

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.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

Allogeneic and autologous transplant

Stem cell (bone marrow) transplants. Allogeneic uses cells from a donor; autologous uses your own cells, collected earlier and given back.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

NYHA class (heart failure)

The New York Heart Association’s four classes of how much heart failure limits physical activity.

I
No limits: ordinary activity causes no undue tiredness or breathlessness.
II
Slight limits: comfortable at rest, ordinary activity causes symptoms.
III
Marked limits: comfortable at rest, less than ordinary activity causes symptoms.
IV
Symptoms even at rest; any activity makes them worse.

Studies set their own limit — many outside heart failure leave out class III–IV, while heart failure studies may ask for a particular class. Check the class this study names.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

COPD

Chronic obstructive pulmonary disease: long-term lung disease that makes it hard to breathe out, including emphysema and chronic bronchitis.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
100 participants (estimated)

Study arms

  • Experimental
    BCD-248

    Drug: BCD-248

Interventions

  • DrugBCD-248

    subcutaneously

06

What researchers measure

Primary outcomes

  1. Overall response rate according to IMWG (International Myeloma Working Group) criteria

    Time frame: Up to 24 weeks

Secondary outcomes

  1. Progression-free survival (PFS)

    Time frame: Up to 104 weeks

  2. Complete response (CR) rate according to IMWG criteria

    Time frame: Up to 3.7 years

  3. MRD (minimal residual disease)-negativity rate

    Time frame: Up to 3.7 years

  4. Duration of response

    Time frame: Up to 3.7 years

  5. Time to progression

    Time frame: Up to 3.7 years

  6. Time to response

    Time frame: Up to 3.7 years

  7. Overall survival

    Time frame: Up to 3.7 years

  8. Incidence and characteristics of adverse events

    Time frame: Up to 3.7 years

  9. Cmax after the first administration

    Time frame: up to Day 6

  10. Cmin after the first administration

    Time frame: up to Day 6

  11. AUC0-t after the first administration

    Time frame: up to Day 6

  12. Ctrough

    Time frame: up to 6 months

  13. Soluble BCMA concentration in the blood

    Time frame: Up to 6 months

  14. Proportion of subjects with BAbs

    Time frame: Up to 3 years

  15. Proportion of subjects with NAbs

    Time frame: Up to 3 years

07

Study locations

7 of 20 sites recruiting
  • State budgetary healthcare institution of the Sverdlovsk region "Sverdlovsk regional clinical hospital №1"
    Ekaterinburg, Russian Federation
    Not yet recruiting
    • Tatiana Konstantinova · Contact
  • SBHI of the Kaliningrad region "Central City Clinical Hospital"
    Kaliningrad, Russian Federation
    Not yet recruiting
    • Alina Chuprakova · Contact
  • SAHI "Republican Clinical Oncology Dispensary of the Ministry of Health of the Republic of Tatarstan named after Professor M.Z. Sigala"
    Kazan, Russian Federation
    Not yet recruiting
    • Gulnara Husainova · Contact
  • FSBI of science "Kirov research Institute of Hematology and blood transfusion of the Federal medical and biological Agency"
    Kirov, Russian Federation
    Not yet recruiting
    • Svetlana Samarina · Contact
  • Regional Government-Owned Publicly Funded Healthcare Institution "Regional Clinical Hospital"
    Krasnoyarsk, Russian Federation
    Recruiting
    • Elena Martynova · Contact
  • Branch of the limited liability company "Hadassah Medical LTD"
    Moscow, Russian Federation
    Recruiting
    • Igor Utiashev · Contact
  • City Clinical Hospital №52 of the Department of Health of the City of Moscow
    Moscow, Russian Federation
    Recruiting
    • Elena Misiurina · Contact
  • FSBI "National Medical Research Center of Oncology named after N. N. Blokhin" of the Ministry of Health of the Russian Federation
    Moscow, Russian Federation
    Not yet recruiting
    • Gaiane Tumian · Contact
  • JSC "Medsi Group of Companies"
    Moscow, Russian Federation
    Recruiting
    • Anastasia Mochalova · Contact
  • SBI of health care of the city of Moscow city clinical hospital named after S. P. Botkin of the Department of health of the City of Moscow
    Moscow, Russian Federation
    Not yet recruiting
    • Vadim Doronin · Contact
  • State budgetary healthcare Institution of the Moscow Region "Moscow Regional Research Clinical Institute named after M. F. Vladimirsky"
    Moscow, Russian Federation
    Not yet recruiting
    • Tatiana Mitina · Contact
  • Federal State Budgetary Institution "National Medical Research Center for Radiology" of the Ministry of Health of the Russian Federation
    Obninsk, Russian Federation
    Not yet recruiting
    • Natalia Falaleeva · Contact
  • SBHI of the Republic of Karelia "Republican Hospital named after V.A. Baranov"
    Petrozavodsk, Russian Federation
    Not yet recruiting
    • Aleksandr Miasnikov · Contact
  • FSBI "Almazov National Medical Research Centre" of the Ministry of Health of the Russian Federation
    Saint Petersburg, Russian Federation
    Recruiting
    • Yurii Osipov · Contact
  • FSBEI of Higher Education "Samara State Medical University" of the Ministry of Health of the Russian Federation
    Samara, Russian Federation
    Not yet recruiting
    • Igor Davidkin · Contact
  • FSBEI HE "Saratov State Medical University named after V.I. Razumovsky" of the Ministry of Health of Russia
    Saratov, Russian Federation
    Recruiting
    • Tatiana Shelekhova · Contact
  • Private healthcare institution "Clinical hospital "RZD-Medicine" of the city of Smolensk"
    Smolensk, Russian Federation
    Not yet recruiting
    • Mariia Novikova · Contact
  • State Budgetary Healthcare Institution "Oncological Dispensary No.2" of the Ministry of Health of the Krasnodar Region
    Sochi, Russian Federation
    Not yet recruiting
    • Dmitrii Kirtbaia · Contact
  • Public institution "Komi Republican cancer clinic"
    Syktyvkar, Russian Federation
    Recruiting
    • Andrei Proidakov · Contact
  • FSBEI of Higher Education "Bashkir State Medical University" of the Ministry of Health of the Russian Federation
    Ufa, Russian Federation
    Not yet recruiting
    • Bulat Bakirov · Contact
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

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 Dec 2024 (actual). Primary completion is estimated for Feb 2026, 14 months after the start.

Of 93 industry-sponsored phase 2 interventional studies under Multiple Myeloma, half reached primary completion within 38 months of starting (the median), counting those still running; a quarter within 27 and three quarters within 77. This study's planned 14 months is below that.

Counting every sponsor, half of 505 studies reached it within 57 months; a quarter within 35 and three quarters within 95.

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

Registered
Oct 30, 2024
First posted
Oct 31, 2024
StartActual
Dec 26, 2024
Primary completionEst.
Feb 2026
CompletionEst.
Jul 2028
Last update
Feb 4, 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 Feb 4, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06668792
Lead sponsor
Biocad
Responsible party
Sponsor
First posted
Oct 31, 2024
Start date
Dec 26, 2024
Primary completion
Feb 2026 (estimated)
Completion
Jul 2028 (estimated)
Last update
Feb 4, 2025

Study contacts

Daria Liaptseva
Contact
liaptseva@biocad.ru
+79816982050

Oversight

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

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