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TanyaKanker
Phase 1NCT07200089Multiple Myeloma
CAR-T cell therapy
CAR-T cell therapy

Recombinant Human IL-7 (NT-I7) in Relapsed/Refractory Multiple Myeloma Following BCMA CAR-T Therapy (Cilta-cel)

CAR-T cell therapy

A Double-blind, Placebo-controlled Phase Ib Study Evaluating the Safety and Toxicity of Recombinant Human IL-7 (NT-I7) in Relapsed/Refractory Multiple Myeloma Following BCMA CAR-T Therapy (Cilta-cel)

Last checked 16 Oktober 2026Source ClinicalTrials.govNCT07200089Not verified

Four separate status dimensions

  • RegistryRecruiting in registry
  • SiteNot verifiedUnknown, so no conclusion can be drawn.
  • International accessUnknownUnknown, so no conclusion can be drawn.
  • Patient matchNot assessedUnknown, so no conclusion can be drawn.

Three statuses often treated as one

A recruiting registry status does not mean a patient can immediately join this study. These three questions are answered by different parties.

  1. Registry status

    Stated by the study record owner: whether the study is listed as recruiting. It does not state whether a site is active.

  2. Site status

    Stated by the facility: whether the site is running this study now. TanyaKanker has not verified this.

  3. International access

    Stated by facility policy: whether patients from outside the local country can be accepted.

Why this appears

Appears because it is recorded for Multiple Myeloma, the treatment category is CAR-T cell therapy.

What to verify

  • • Acceptance of patients from outside the local country has not been verified.
  • • We have not verified that the study site is actively running this study.
  • • Eligibility is determined by the study team, not by registry data.
  • • This record has never been directly verified by us.
Upload Medical ReportsRegistry ClinicalTrials.gov

Preliminary screening only shows overlap and data needs. Eligibility is determined by the study team.

Why this study may be relevant

  • This study is recorded for Multiple Myeloma, the same cancer group you are exploring.
  • Recorded interventions: NT-I7, Placebo.
  • The study is in Phase 1 according to registry data.
  • Locations are recorded in United States.

The relevance above is assembled from registry data, not from an eligibility judgement.

Study basis

A Double-blind, Placebo-controlled Phase Ib Study Evaluating the Safety and Toxicity of Recombinant Human IL-7 (NT-I7) in Relapsed/Refractory Multiple Myeloma Following BCMA CAR-T Therapy (Cilta-cel)

Sponsor
Washington University School of Medicine
Registry
ClinicalTrials.gov NCT07200089
Phase
Phase 1

Cancer and markers

Multiple Myeloma

Recorded interventions

NT-I7Placebo

Study locations

  • Washington University School of Medicine

    St Louis

    United States

What we know

  • Registry status: Recruiting.
  • Phase 1 with sponsor Washington University School of Medicine.
  • 1 locations recorded in the registry.
  • Registry data updated 2026-10-15.

What we do not know yet

  • Whether the site accepts patients from outside the local country.
  • Whether the site is actively running the study now.
  • Which cost components are borne by participants.
  • Which documents the sponsor requires.

Main eligibility factors from the registry

  • Protocol sex: all
  • Protocol minimum age: 18 Years
  • Complete eligibility criteria appear only in the study protocol and must be assessed by the study team.

This summary is taken from registry data. Complete criteria live in the study protocol and must be assessed by the study team.

Documents that may be needed

  • Disease history summary from the treating doctor
  • Most recent pathology report
  • Molecular marker report if available
  • Most recent imaging results
  • List of current medicines

This is a general frame, not the sponsor's official list.

Upload Medical Reports

Updates and sources

Registry update
2026-10-15
Retrieved by TanyaKanker
2026-10-16
Last verified
Never
Contact status
Not contacted

Data comes from the public ClinicalTrials.gov registry of the US National Library of Medicine. Registry facts are public data; interpretation about international patient access, cost, and site readiness does NOT come from the registry and is marked unverified.

https://clinicaltrials.gov/study/NCT07200089

Treatment categories

Cost

NOT VERIFIED

Not verified. The public registry does not include cost details for international patients and does not state payment coverage.

This information is not a diagnosis or a medical recommendation. Decisions remain with your medical team.

Not a diagnosis and not final medical advice. Must be reviewed by a doctor.

Other studies in a similar group

Check preliminary match for your case

This screening shows overlap between your summary and the study, plus data that still needs to be completed. Eligibility remains the study team's decision.

Consult via WhatsAppUpload Medical Reports

After submission, a human navigator reviews your request and contacts you through your chosen channel. The WhatsApp message already includes this page context, so you do not need to explain from the beginning.

Clinical data is not requested in the form and is not sent to analytics. Do not send medical reports through WhatsApp or email; use the secure upload page. We do not promise eligibility or any treatment outcome.

Next steps

These suggestions come from links between entries in TanyaKanker's database, not from a medical judgement. Each suggestion includes why it appears.

To check

What you can do

  • Upload medical reports

    Build a case summary in twelve steps

    Reason: Often the most useful next step after reading this page

  • Request a second opinion

    Review of the treatment plan

    Reason: Relevant when a treatment plan is being considered

  • Consult a navigator

    A request is recorded with this page context

    Reason: For asking the next step directly

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