Clinical Trials
Every treatment that has ever made a difference in cancer care was once a part of a clinical trial. MUSC Hollings Cancer Center is committed to offering the best treatments available today while searching for even better ones for the future. Ask your doctor if a clinical trial is right for you.
Sarcoma Trials
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STUDY17022
First in Human, Phase 1/1b, Open label, Multicenter Study of Bifunctional EGFR/TGF ß Fusion Protein BCA101 Monotherapy and in Combination Therapy in Patients with EGFR Driven Advanced Solid Tumors
The investigational drug to be studied in this protocol, BCA101, is a first-in-class compound that targets both EGFR with TGFβ. Based on preclinical data, this bifunctional antibody may exert synergistic activity in patients with EGFR-driven tumors.
Study Information
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STUDY21361
A Phase 1/2 Open label, Multicenter Study to Assess the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of PC14586 in Patients with Advanced Solid Tumors Harboring a p53 Y220C Mutation (PYNNACLE)
This study will assess the safety and tolerability of multiple dose levels of PC14586 in participants with advanced solid tumors containing a p53 Y220C mutation.
Study Information
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STUDY21565
A Study of E7386 in Combination With Other Anticancer Drug in Participants With Solid Tumor (Endometrial cohort enrolling 2nd and 3rd line patients.)
To assess safety and tolerability and to determine the recommended Phase 2 dose (RP2D) of
E7386 in combination with other anticancer drug(s). To assess pharmacokinetic (PK) profile of study drug(s)
To assess efficacy (objective response rate [ORR], best overall response [BOR], disease control
rate [DCR], clinical benefit rate [CBR], progression-free survival [PFS], overall survival [OS],
and duration of response [DOR]) of E7386 in combination with other anticancer drug(s)
(Revised per Amendment 06)
Study Information
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STUDY21654
Feasibility Trial of Preoperative 5 Day Hypofractionated Radiotherapy for Primary Soft Tissue Sarcoma
To determine the feasibility of preoperative 5-day HFRT for extremity STS within the HCC patient population
Secondary Objectives:
To evaluate the rates of favorable pathologic response, major woundcomplications, local control, acute toxicity, and 1-year late toxicity
associated with preoperative 5-day HFRT
Exploratory Objectives:
To compare the socio-demographic profile of trial participants with those
of extremity STS patients who would have meet trial criteria and were
offered preoperative CFRT in the 3 years prior to the study opening at HCC
To compare the retention rate for radiotherapy at HCC in patients meeting
trial criteria during the prior 3 years with the retention rate for
radiotherapy during the study period
To compare serum levels of SFRP2 before and after preoperative 5-day
HFRT
To evaluate changes in serum SFRP2 levels before and after preoperative
5-day HFRT for an association with favorable pathologic response
To evaluate patient satisfaction with the decision to participate in a trial of
preoperative 5-day HFRT
To assess the importance of the shorter duration of radiotherapy in an
individual patient s decision to participate in the study
Study Information
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STUDY21774
A Phase 1/2, First-In-Human, Multi-Part, Open-Label Study to Investigate the Safety, Tolerability, Pharmacokinetics, Biological and Clinical Activity of DF9001 as a Monotherapy and in Combination with Nivolumab in Patients With Advanced (Unresectable, Recurrent, or Metastatic) Solid Tumors, and Expansion in Selected Indications
Determine the maximum tolerated dose (MTD) of DF9001 as a monotherapy and in combination with nivolumab in participants with advanced (unresectable, recurrent, or metastatic) solid tumors. Assess the overall response rate (ORR) according to the Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1) per an Independent Endpoint Review Committee (IERC).
Study Information