Phase 2 Peripheral Arterial Disease Trial, Recruiting NCT06849986 Sponsor: Fudan University Condition: Peripheral Arterial Disease
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Phase 2 Peripheral Arterial Disease Trial, Recruiting

NCT06849986
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:

  • You are between 18 and 75 years old (any gender)
  • You have been diagnosed with one of these specific types of soft tissue sarcoma, confirmed by a tissue sample test: undifferentiated sarcoma (except small round cell type), synovial sarcoma, angiosarcoma, fibrosarcoma, smooth muscle sarcoma, liposarcoma (except well-differentiated type), pleomorphic rhabdomyosarcoma, malignant peripheral nerve sheath tumor, desmoplastic small round cell tumor, NOS sarcoma, SMARCA4-deficient sarcoma, malignant phyllodes tumor of the breast, or intimal sarcoma
  • Your cancer has spread or come back and cannot be treated with surgery or radiation therapy
  • You are generally able to carry out daily activities with little to no limitation (confirm with trial site)
  • Doctors expect you to live for more than 3 months
  • Your recent blood tests (within the last 7 days) show that your blood cell counts, liver function, and kidney function are within acceptable ranges (confirm with trial site for specific values)
  • Your cancer can be measured on scans according to standard medical guidelines
  • You (or your legal representative) are willing to sign a consent form agreeing to take part in the study

Who may not be able to join:

  • You have previously received treatment for advanced soft tissue sarcoma, unless your cancer came back more than 6 months after completing a lower-dose course of a specific chemotherapy drug called doxorubicin
  • You have received any experimental or cancer-fighting drugs within the 4 weeks before joining the trial
  • You have previously been treated with certain immune checkpoint or T-cell targeting drugs (such as anti-PD-1, anti-PD-L1, anti-CTLA-4, or similar therapies)
  • You have had another type of cancer in the past 5 years, unless it was cervical cancer or skin basal cell carcinoma that has been fully cured
  • You have brain or nervous system (meningeal) metastases that are currently causing symptoms, unless they were treated successfully more than 6 months ago and have been stable since
  • You are currently experiencing significant active bleeding
  • You are pregnant or breastfeeding, or are able to become pregnant and have not been using adequate contraception
  • You have a problem with alcohol abuse or drug addiction
  • You have an active autoimmune disease (such as lupus, rheumatoid arthritis, inflammatory bowel disease, multiple sclerosis, or similar conditions), or a history of one that could come back — or you are at high risk due to a previous organ transplant requiring immune-suppressing medication (note: certain mild conditions like thyroid hormone replacement or skin conditions not needing systemic treatment may still be eligible — confirm with trial site)
  • You need to take high-dose steroid medications (such as prednisone above a certain level) or other immune-suppressing drugs within 14 days before or during the trial (short-term or inhaled/topical steroids for non-autoimmune conditions may be acceptable — confirm with trial site)
  • You have had serious heart or lung problems, such as a heart attack, heart failure, unstable chest pain, serious irregular heartbeat, or interstitial lung disease within the past 6 months
  • You have HIV, another immune deficiency condition, or have had an organ or stem cell transplant
  • You have active hepatitis B or active hepatitis C (note: people who are stable carriers of hepatitis B on treatment, or who have been fully cured of hepatitis C, may still be eligible — confirm with trial site)
  • You have a serious neurological or psychiatric condition, a severe active infection, a serious blood clotting disorder, or any other condition that the doctors believe would put you at risk or prevent you from completing the study

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 23 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

Phone: +86 13761503356

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
Registry
ClinicalTrials.gov
Start date
25 February 2025
Est. completion
31 December 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

ORR

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: 23 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