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Discovery of molecular signatures to understand the response of Immuno-oncology drugs

Identification of resistance and response markers to immuno-oncology drugs. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/09/057273
Enrollment
100
Registered
2023-09-06
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: C50-C50- Malignant neoplasms of breast Health Condition 2: C15-C26- Malignant neoplasms of digestive organs Health Condition 3: C51-C58- Malignant neoplasms of female genital organs Health Condition 4: C00-C14- Malignant neoplasms of lip, oral cavity and pharynx Health Condition 5: C45-C49- Malignant neoplasms of mesothelial and soft tissue Health Condition 6: C30-C39- Malignant neoplasms of respiratory and intrathoracic organs Health Condition 7: C64-C68- Malignant neoplasms

Interventions

Intervention1: Nil: Nil

Sponsors

Strand Life Sciences Pvt Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with confirmed malignant carcinoma as defined above who are eligible for mono-immuno-oncology therapy and will undergo the treatment, as identified by the site Principal Investigator or Co-Investigators through routine clinical care processes Age - 18 years and above Both men and women of all races and ethnic groups are eligible for this study New, relapsed, recurrent or metastatic cases Ability to understand and the willingness to sign a written Informed Consent Form

Exclusion criteria

Exclusion criteria: Pregnant or lactating women Patients who have untreated active infection Patients who are receiving any additional oncology investigational agent(s) with immuno-oncology drugs Patients undergoing combinatorial immunotherapy

Design outcomes

Primary

MeasureTime frame
Identification of signature biomarkers via a minimally invasive procedure will enable distinguishing between mono immunooncology drug responder & nonresponder or patient prognosis while on mono immunotherapy for cancer.Timepoint: 13 (before therapy starts and every month for period of 12 months)

Secondary

MeasureTime frame
Identification of reliable predictive molecular markers to distinguish responders & non-responders for immuno-oncology drugsTimepoint: 13 (before therapy starts & every month for period of 12 months)

Countries

India

Contacts

Public ContactDr Vamsi Veeramachaneni

Strand Life Sciences Pvt Ltd

vamsi@strandls.com918023095299

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026