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Prophylaxis of Complications of Basic Therapy Using Naderin in Socially Significant Diseases (NADERIN-SSD)

26 de junho de 2026 atualizado por: MIPO Clinic

Prophylaxis of Complications of Basic Therapy and Medical Rehabilitation Using Naderin in Socially Significant Diseases, Including Malignant Neoplasms, Tuberculosis, and Hepatitis C

This interventional study evaluated the efficacy of Naderin (sodium nucleinate) for the prophylaxis of complications during basic therapy and medical rehabilitation in patients with socially significant diseases, including malignant neoplasms, tuberculosis, and hepatitis C. The study assessed the immunocorrective effects of Naderin on hematological parameters, the incidence of infectious complications, and clinical outcomes.

A total of 75 patients (40 in the main group and 35 in the control group) were enrolled. Patients in the main group received Naderin as an adjunct to standard therapy, while the control group received standard therapy without immunocorrection. The study demonstrated that Naderin reduced the duration of neutropenia by 4-5 days, attenuated the decline in white blood cell and lymphocyte counts during chemotherapy, and reduced the incidence of treatment interruptions due to complications. These findings suggest that Naderin may serve as an effective immunomodulatory agent for supportive care in patients with socially significant diseases.

Visão geral do estudo

Descrição detalhada

Rationale Standard treatments for malignant neoplasms, tuberculosis, and hepatitis C may be associated with clinically important complications (e.g., cytopenias, immunosuppression, infections) that can impair treatment delivery and rehabilitation. Naderin (sodium nucleinate) was evaluated as an adjunct immunomodulatory/supportive-care approach intended to improve tolerance of basic therapy and reduce complication-related disruptions.

Study Design and Setting This was a prospective, controlled, open-label interventional study conducted at clinical sites affiliated with the Kazakh National Medical University (KazNMU), Almaty, Kazakhstan, supported by KazNMU Grant 2013. Allocation to intervention vs control was non-randomized (controlled cohort comparison).

Study Population and Groups (high-level)

A total of 75 participants with one of the following diagnostic categories were enrolled: malignant neoplasms, tuberculosis, or hepatitis C. Participants were assigned to:

  • Intervention group: standard-of-care therapy for the underlying condition plus Naderin (immunocorrection).
  • Control group: standard-of-care therapy without Naderin. (Condition-specific eligibility criteria and any stratification by disease category should be presented in the Eligibility Criteria and Study Design/Arms sections rather than repeated here.) Intervention (high-level description) Participants in the intervention group received Naderin (sodium nucleinate) as an adjunct to standard therapy. Key intervention specifications should be captured in the Arms/Interventions module (and/or here if not elsewhere): route, dose, frequency, timing relative to basic therapy, duration, and criteria for dose modification/discontinuation, consistent with protocol reporting standards for reproducibility 1.

Assessments and Follow-up

Participants underwent baseline and follow-up assessments during the active treatment/rehabilitation period that included:

  • Hematology monitoring (e.g., WBC and lymphocyte counts; other CBC indices as applicable to the disease group and therapy).
  • Clinical surveillance for infectious complications using predefined clinical criteria and documentation of antimicrobial treatment/hospitalization where relevant.
  • Documentation of basic-therapy delivery (e.g., interruptions, delays, or discontinuation attributable to complications).
  • Safety monitoring for adverse events temporally associated with adjunctive Naderin and with underlying disease therapy.

Outcomes (high-level; details elsewhere) The study evaluated hematologic parameters, infectious complications, treatment delivery disruption due to complications, and rehabilitation-related clinical outcomes. Outcome definitions, metrics, and time frames should be specified in the dedicated Outcome Measures section per SPIRIT guidance 1 and SPIRIT-Outcomes extension expectations for prespecification 2.

Statistical Approach (high-level) Between-group comparisons were planned using appropriate tests based on outcome type (categorical vs continuous) with a prespecified two-sided significance threshold. If subgroup analyses by disease category (neoplasm vs TB vs HCV) were planned, the analysis set and handling of multiplicity should be stated in the Statistical Analysis Plan or briefly here with a reference, consistent with SPIRIT expectations 1.

Ethics and Oversight The study received ethics approval from the Local Ethics Committee of KazNMU (Approval No. 15678). Written informed consent was obtained prior to enrollment. No data monitoring committee was constituted.

Tipo de estudo

Intervencional

Inscrição (Real)

75

Estágio

  • Fase 2
  • Fase 3

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

  • Diagnosis of malignant neoplasm, tuberculosis, or hepatitis C (confirmed by clinical, laboratory, and/or histopathological criteria)
  • Age between 18 and 50 years at the time of enrollment
  • Receiving standard basic therapy (chemotherapy, anti-tuberculosis therapy, or antiviral therapy) according to national clinical protocols
  • Signed informed consent to participate in the study
  • Willingness to comply with study procedures and follow-up visits
  • ECOG performance status ≤ 2 or equivalent

Exclusion Criteria:

  • Severe concomitant diseases (e.g., decompensated cardiovascular, renal, or hepatic failure) that could interfere with study participation or outcome assessment
  • Known hypersensitivity or contraindications to Naderin (sodium nucleinate) or its components
  • Pregnancy or lactation
  • Participation in any other interventional clinical trial within 30 days prior to enrollment
  • Active or uncontrolled infections (other than the primary study condition)
  • Severe immunodeficiency (e.g., HIV/AIDS, advanced hematological malignancies) not related to the primary study condition
  • Mental or cognitive impairment that would preclude informed consent or compliance with study procedures
  • History of organ transplantation requiring immunosuppressive therapy
  • Any other condition that, in the investigator's opinion, would make the participant unsuitable for the study

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Cuidados de suporte
  • Alocação: Não randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Solteiro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Naderin + Standard Therapy
Participants received standard basic therapy for their underlying disease (malignant neoplasms, tuberculosis, or hepatitis C) in combination with Naderin (sodium nucleinate) as an adjunct immunocorrective therapy for the prophylaxis of complications.
Naderin (sodium nucleinate) is an immunomodulatory agent administered as an adjunct to standard basic therapy for the prophylaxis of complications. It enhances immune function, reduces the duration of neutropenia, and attenuates the decline in hematological parameters during chemotherapy and other aggressive therapies.
Outros nomes:
  • nucleinato de sódio
Comparador Ativo: Standard Therapy Alone
Participants received standard basic therapy for their underlying disease (malignant neoplasms, tuberculosis, or hepatitis C) without immunocorrection.
Standard basic therapy according to clinical protocols for malignant neoplasms, tuberculosis, and hepatitis C. Includes chemotherapy, anti-tuberculosis therapy, and antiviral therapy as per national guidelines.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Incidence of Infectious Complications
Prazo: Up to 6 months (from study start to completion)
The number and proportion of participants who developed infectious complications (e.g., pneumonia, febrile neutropenia, bacterial infections) during the course of basic therapy (chemotherapy, anti-tuberculosis therapy, antiviral therapy).
Up to 6 months (from study start to completion)
Duration of Neutropenia
Prazo: Up to 6 months (from study start to completion)
The number of days participants experienced neutropenia (absolute neutrophil count < 1.0 × 10⁹/L) during the course of basic therapy.
Up to 6 months (from study start to completion)
Change in White Blood Cell (WBC) and Lymphocyte Counts
Prazo: Baseline and up to 6 months
The change in white blood cell count (× 10⁹/L) and lymphocyte count (× 10⁹/L) from baseline to post-treatment assessment, comparing the Naderin group and control group.
Baseline and up to 6 months

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Time to Recovery of Hematological Parameters
Prazo: Up to 6 months
The number of days required for normalization of white blood cell count, lymphocyte count, and absolute neutrophil count after the completion of therapy.
Up to 6 months
Adverse Events Profile
Prazo: Up to 6 months
The number and severity of adverse events (graded according to CTCAE criteria) experienced by participants in both groups.
Up to 6 months
Duration of Hospitalization
Prazo: Up to 6 months
The total number of days participants were hospitalized during the course of therapy and follow-up
Up to 6 months

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

15 de maio de 2013

Conclusão Primária (Real)

21 de setembro de 2013

Conclusão do estudo (Real)

12 de março de 2014

Datas de inscrição no estudo

Enviado pela primeira vez

22 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

22 de junho de 2026

Primeira postagem (Real)

26 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

30 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

26 de junho de 2026

Última verificação

1 de junho de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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