Phase 2 Type 1 Diabetes Trial, Recruiting NCT03356782 Sponsor: Shenzhen Geno-Immune Medical Institute Condition: Type 1 Diabetes
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Phase 2 Type 1 Diabetes Trial, Recruiting

NCT03356782
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People diagnosed with Stage III or Stage IV sarcoma, or sarcoma that has come back after previous treatment
  • People aged 18 to 65 years old at the time of joining the trial
  • People who have waited at least 4 weeks since their last chemotherapy or radiation treatment, and at least 1 week since any immune-suppressing medications (such as steroid hormones)
  • People whose side effects from previous chemotherapy have been well managed
  • People whose cancer cells test positive for a specific target (confirmed by laboratory testing)
  • People with a general health and activity score of 50% or higher on a standard medical scale (confirm with trial site)
  • People with a life expectancy of more than 6 weeks
  • People whose blood cell counts meet the minimum required levels for white blood cells and platelets (confirm with trial site for exact values)
  • People whose blood oxygen level is 90% or above when breathing normal room air
  • People whose liver function tests fall within acceptable ranges, as determined by the trial doctors
  • People whose kidney function tests fall within acceptable ranges, as determined by the trial doctors
  • People whose own immune T cells can be successfully prepared at the required level for the treatment (confirm with trial site)
  • People who are willing to sign a consent form agreeing to take part

Who may not be able to join:

  • People whose disease is progressing very rapidly
  • People currently receiving another new or experimental treatment
  • People whose tumour may be blocking or at risk of blocking their airway
  • People with a history of epilepsy or other conditions affecting the brain or nervous system
  • People who need immune-suppressing medications due to graft-versus-host disease (a reaction sometimes seen after certain medical procedures)
  • People with a history of a heart condition called long QT syndrome, or other serious heart disease
  • People with an active infection that is not under control
  • People with active hepatitis B, hepatitis C, or HIV infection
  • People who have been taking steroid medications throughout their whole body (not inhaled) within the 2 weeks before joining
  • People who have previously received any gene therapy treatment
  • People whose kidney or liver function test results fall outside specific limits set by the trial (confirm with trial site for exact values)
  • People with other serious uncontrolled health conditions that would prevent safe participation
  • People who are pregnant or breastfeeding
  • People who have previously had a bad reaction to the drug cyclophosphamide
  • People whose sarcoma has spread to the brain or central nervous system
  • People whose situation may present risks to their safety or interfere with the trial results (confirm with trial site)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 21 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Lung-Ji Chang, PhD, Shenzhen Geno-Immune Medical Institute

Phone: +86 0755-86573763

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Shenzhen Geno-Immune Medical Institute
Registry
ClinicalTrials.gov
Start date
1 June 2026
Est. completion
31 December 2029

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Safety of CART cells in patients using CTCAE version 4.0 standard to evaluate the level of adverse events

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov