Trial · NCT05483933
Results by group124
Each measurement the trial posted, group by group, in the words and numbers it posted.
1 to 20 of 124
Download this page as JSON| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Evaluate Safety and Tolerability of SL-172154 When Administered With PLD or Mirvetixumab | Pegylated Liposomal Doxorubicin + SL-172154 | 20 | Participants | ||
| Evaluate Safety and Tolerability of SL-172154 When Administered With PLD or Mirvetixumab | Mirvetixumab + SL-172154 | 65 | Participants | ||
| To Assess Preliminary Evidence of Anti-tumor Activity of SL-172154 When Administered With PLD or Mirvetixumab | Pegylated Liposomal Doxorubicin + SL-172154 | Complete response | 0 | Participants | |
| To Assess Preliminary Evidence of Anti-tumor Activity of SL-172154 When Administered With PLD or Mirvetixumab | Mirvetixumab High (PS2+ ≥75%) + SL-172154 | Complete response | 1 | Participants | |
| To Assess Preliminary Evidence of Anti-tumor Activity of SL-172154 When Administered With PLD or Mirvetixumab | Mirvetixumab Low+Medium ((PS2+ ≥25% to <75%) + SL-172154 | Complete response | 0 | Participants | |
| To Assess Preliminary Evidence of Anti-tumor Activity of SL-172154 When Administered With PLD or Mirvetixumab | Pegylated Liposomal Doxorubicin + SL-172154 | Partial response | 4 | Participants | |
| To Assess Preliminary Evidence of Anti-tumor Activity of SL-172154 When Administered With PLD or Mirvetixumab | Mirvetixumab High (PS2+ ≥75%) + SL-172154 | Partial response | 12 | Participants | |
| To Assess Preliminary Evidence of Anti-tumor Activity of SL-172154 When Administered With PLD or Mirvetixumab | Mirvetixumab Low+Medium ((PS2+ ≥25% to <75%) + SL-172154 | Partial response | 4 | Participants | |
| To Assess Preliminary Evidence of Anti-tumor Activity of SL-172154 When Administered With PLD or Mirvetixumab | Pegylated Liposomal Doxorubicin + SL-172154 | Stable Disease | 10 | Participants | |
| To Assess Preliminary Evidence of Anti-tumor Activity of SL-172154 When Administered With PLD or Mirvetixumab | Mirvetixumab High (PS2+ ≥75%) + SL-172154 | Stable Disease | 21 | Participants | |
| To Assess Preliminary Evidence of Anti-tumor Activity of SL-172154 When Administered With PLD or Mirvetixumab | Mirvetixumab Low+Medium ((PS2+ ≥25% to <75%) + SL-172154 | Stable Disease | 13 | Participants | |
| To Assess Preliminary Evidence of Anti-tumor Activity of SL-172154 When Administered With PLD or Mirvetixumab | Pegylated Liposomal Doxorubicin + SL-172154 | Progressive Disease | 6 | Participants | |
| To Assess Preliminary Evidence of Anti-tumor Activity of SL-172154 When Administered With PLD or Mirvetixumab | Mirvetixumab High (PS2+ ≥75%) + SL-172154 | Progressive Disease | 5 | Participants | |
| To Assess Preliminary Evidence of Anti-tumor Activity of SL-172154 When Administered With PLD or Mirvetixumab | Mirvetixumab Low+Medium ((PS2+ ≥25% to <75%) + SL-172154 | Progressive Disease | 9 | Participants | |
| To Assess Preliminary Evidence of Anti-tumor Activity of SL-172154 When Administered With PLD or Mirvetixumab | Pegylated Liposomal Doxorubicin + SL-172154 | Not Evaluable | 0 | Participants | |
| To Assess Preliminary Evidence of Anti-tumor Activity of SL-172154 When Administered With PLD or Mirvetixumab | Mirvetixumab High (PS2+ ≥75%) + SL-172154 | Not Evaluable | 0 | Participants | |
| To Assess Preliminary Evidence of Anti-tumor Activity of SL-172154 When Administered With PLD or Mirvetixumab | Mirvetixumab Low+Medium ((PS2+ ≥25% to <75%) + SL-172154 | Not Evaluable | 0 | Participants | |
| Immunogenicity to SL-172154 | Pegylated Liposomal Doxorubicin + SL-172154 | 0 | Participants | ||
| Immunogenicity to SL-172154 | Mirvetuximab + SL-172154 | 38 | Participants | ||
| Immunogenicity to MIRV | Mirvetuximab + SL-172154 | 8 | Participants |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
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GET https://conductscience.org/api/trials/v1/NCT05483933/results