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An invasive ductal carcinoma clinical trial can provide a patient with a unique opportunity to be among the first people to benefit from a promising new breast cancer treatment that is not yet available in other settings. Through these important research studies, scientists and clinicians gain the information they need to determine whether new treatment options are more effective, or equally effective but produce fewer side effects, than the prevailing standard of care. If a treatment under evaluation in a clinical trial demonstrates better results than the treatment it is being compared to, the emerging treatment may become the new standard. In fact, all currently available treatment options were once available only through clinical trials.

With that said, a decision to participate in a breast cancer clinical trial should not be made lightly. After exploring all possible treatment options with a physician, a patient is encouraged to talk with family members and trusted friends. Ultimately, though, after gathering and reviewing all available information, only the patient can decide whether a specific trial is the right path to take.

Prior to enrolling in an invasive ductal carcinoma clinical trial, a patient should:

  • Learn all about the trial, including its risks and benefits, what may happen and the costs involved, if any
  • Understand the scope of informed consent (leaving the study at any time is always an option)
  • Consider the extra time requirements (traveling to and from the study site, maintaining a log, etc.)

As a National Cancer Institute-designated Comprehensive Cancer Center, Moffitt Cancer Center is a recognized leader that continues to pave the way for breast cancer research. Through the groundbreaking clinical trials being performed in our Don & Erika Wallace Comprehensive Breast Program, our patients can potentially experience improved outcomes while making important contributions to the growing base of scientific knowledge, which can ultimately benefit all present and future breast cancer patients.

If you’d like to learn more about possibly participating in an invasive ductal carcinoma clinical trial, our clinical trial navigators can answer your questions and provide further information. Call 1-813-745-6100 or 1-800-679-0775 (toll-free) or submit a clinical trials inquiry form online. No referrals are required.

 

  • Clinical Trials

    CLINICAL TRIAL 16933
    Older Breast Cancer Patients: Risk For Cognitive Decline
    Condition: Breast
    Intervention:

    CLINICAL TRIAL 19000
    Evaluation of Anti-Her2 and Anti-Her3 T-Helper Response in Primary Breast Cancer
    Condition: Breast
    Intervention: Not Applicable ()

    CLINICAL TRIAL 19209
    Combined Imaging and Blood Biomarkers for Breast Cancer Diagnosis
    Condition: Healthy Subjects
    Intervention:

    CLINICAL TRIAL 19646
    Prospective Observational Cohort Study of Patients with Metastatic HER-2+ Breast Cancer at Risk of Cardiac Toxicity
    Condition: Breast
    Intervention: Carvedilol (); Not Applicable ()

    CLINICAL TRIAL 20030
    TAILOR RT: A Randomized Trial of Regional Radiotherapy in Biomarker Low Risk Node Positive and T3N0 Positive Breast Cancer
    Condition: Breast
    Intervention: Not Applicable ()

    CLINICAL TRIAL 20487
    Phase I/II Study of Radiation Therapy Followed by Intrathecal Trastuzumab/Pertuzumab in the Management of HER2+ Breast Leptomeningeal Disease
    Condition: Breast
    Intervention: Herceptin (Trastuzumab); Pertuzumab (); Radiotherapy (); Trastuzumab (); rhuMAb HER2 (Trastuzumab)

    CLINICAL TRIAL 20899
    Phase I/II Study of Stereotactic Radiation and Abemaciclib with or without Imlunestrant in the Management of Hormone Receptor Positive HER2 Negative Breast Cancer Brain Metastases (STRONG Trial)
    Condition: Breast
    Intervention: Abemaciclib (); Endocrine Therapy (); Imlunestrant (); LY2835219 (Abemaciclib); Radiotherapy ()

    CLINICAL TRIAL 20897
    Phase 1 Dose-Escalation, Dose-Expansion Trial of Intratumoral HER2- and HER3-Primed Dendritic Cells Injections for the Treatment of Early-Stage TNBC and ER Low Positive Breast Cancer (DecipHER)
    Condition: Breast
    Intervention: Adriamycin (doxorubicin); DC1 Vaccine (); Neulasta (pegfilgrastim); Paraplatin (carboplatin); Pembrolizumab (Keytruda); Taxol (paclitaxel); carboplatin (); cyclophosphamide (); cytoxan (cyclophosphamide); paclitaxel (); pegfilgrastim ()

    CLINICAL TRIAL 20915
    Neoadjuvant Therapy of HER2 directed Dendritic Cell (DC1) vaccine Plus Weekly Paclitaxel, Trastuzumab and Pertuzumab in Patients with HER-2 Positive Breast Cancer (NATASHA trial)
    Condition: Breast
    Intervention: DC1 Vaccine (); Herceptin (Trastuzumab); Pertuzumab (); Taxol (paclitaxel); Trastuzumab (); paclitaxel (); rhuMAb HER2 (Trastuzumab)

    CLINICAL TRIAL 21093
    Phase 1/1b/2 Multicenter, Open-Label, First-in-Human Dose Escalation and Dose Expansion Study to Assess Safety and Tolerability of Orally Administered PMD-026 as a Single Agent and in Combination in Patients with Metastatic or Locally Advanced (Inoperable) RSK2+ Breast Cancer
    Condition: Breast
    Intervention: Faslodex (fulvestrant); PMD-026 (); fulvestrant ()

    CLINICAL TRIAL 21378
    Phase 1 Study of Adoptive T Cell Therapy Following HER2-Pulsed Dendritic Cell Vaccine and Pepinemab / Trastuzumab in Patients with Metastatic HER2-Positive Breast Cancer
    Condition: Breast
    Intervention: CD4+ T Cells (); DC1 Vaccine (); Herceptin (Trastuzumab); Pepinemab (VX15/2503); Trastuzumab (); cyclophosphamide (); cytoxan (cyclophosphamide); rhuMAb HER2 (Trastuzumab)

    CLINICAL TRIAL 21589
    BASECAMP-1: An Observational Study Obtaining Solid Tumor Tissue from Subjects with Primary Surgical Resection and Leukapheresis for CAR T-Cell Therapy Manufacturing
    Condition: Immunotherapy
    Intervention:

    CLINICAL TRIAL 21673
    A Randomized, Multicenter, Placebo-controlled, Phase 3 study to Evaluate the Efficacy and Safety ofHER2/neu Peptide GLSI-100 (GP2 + GM-CSF) in HER2/neu Positive Subjects with Residual Disease or High-Risk PCR After Both Neoadjuvant and Postoperative Adjuvant Trastuzumab-Based Therapy (FLAMINGO-01)
    Condition: Breast
    Intervention: GLSI-100 (); Placebo ()

    CLINICAL TRIAL 21676
    Phase I/II Study of Stereotactic Radiation and Sacituzumab Govitecan with Zimberelimab in the Management of Metastatic Triple Negative Breast Cancer with Brain Metastases (TARGET-TNBC)
    Condition: Breast
    Intervention: Sacituzumab Govitecan (); Zimberelimab ()

    CLINICAL TRIAL 21757
    Phase II Study of Genomically Guided Radiation Dose Personalization in the Management of Triple Negative Breast Cancer
    Condition: Breast
    Intervention: Radiotherapy ()

    CLINICAL TRIAL 21899
    Phase Ib Expansion Study of CX-5461 in Patients with Solid Tumours and BRCA2 and/or PALB2 Mutation
    Condition: Multiple
    Intervention: CX-5461 ()

    CLINICAL TRIAL 22102
    A Phase 1b, First-in-human, Dose Escalation and Expansion, Multicenter Study of XMT-1660 in Participants with Solid Tumors
    Condition: Multiple
    Intervention: XMT-1660 ()

    CLINICAL TRIAL 17268-B
    I-SPY 2.2 TRIAL - Investigation of Serial Studies to Predict your Therapeutic Response with Imaging and Molecular Analysis 2
    Condition: Breast
    Intervention: AKTi (); AMP-514 (Durvalumab); ARV-471 (); ARX-788 (); Abemaciclib (); Adriamycin (doxorubicin); Cemiplimab (); DAN-222 (); Datopotamab Deruxtecan (); Dostarlimab (); Durvalumab (); Femara (Letrozole); GSK5733584 (); Herceptin (Trastuzumab); LY2835219 (Abemaciclib); Lasofoxifene (); Letrozole (); MEDI4736 (Durvalumab); Niraparib (); PD-1 (); PD-L1 (); Paraplatin (carboplatin); Pembrolizumab (Keytruda); Pertuzumab (); REGN2810 (Cemiplimab); Rilvegostomig (); Sarilumab (); T-Dxd (); TSR-042 (Dostarlimab); Taxol (paclitaxel); Taxotere (docetaxel); Trastuzumab (); VV1 (); Z-endoxifen (); Zanidatamab (); carboplatin (); cyclophosphamide (); cytoxan (cyclophosphamide); docetaxel (); doxorubicin (); paclitaxel (); rhuMAb HER2 (Trastuzumab)

    CLINICAL TRIAL 22305
    First-in-Human Study of STX-478, a Mutant-Selective PI3Ka Inhibitor as Monotherapy and in Combination with Other Antineoplastic Agents in Participants With Advanced Solid Tumors
    Condition: Multiple
    Intervention: 772256 (Palbociclib); Abemaciclib (); Anastrozole (); Arimadex (Anastrozole); Aromasin (Exemestane); Exemestane (); Faslodex (fulvestrant); Femara (Letrozole); Imlunestrant (); LEE011 (Ribociclib); LY2835219 (Abemaciclib); Letrozole (); Palbociclib (); Ribociclib (); STX478-101 (); fulvestrant ()

    CLINICAL TRIAL 22356
    A Modular Open-Label, Multi-Centre Phase 1/2 Dose-Finding, Optimistation, and Expansion Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of EP0062 in Patients with Relapsed Locally Advanced or Metastatic AR+/HER2-/ER+ Breast Cancer
    Condition: Breast
    Intervention: 772256 (Palbociclib); Abemaciclib (); Aromasin (Exemestane); EP0062 (); Elacestrant (); Exemestane (); Faslodex (fulvestrant); LEE011 (Ribociclib); LY2835219 (Abemaciclib); Palbociclib (); Ribociclib (); everolimus (RAD001); fulvestrant ()

    CLINICAL TRIAL 22515
    Genomic Alterations of PI3K Pathway in HER2-Positive Breast Cancer
    Condition: Breast
    Intervention:

    CLINICAL TRIAL 22617
    A Pilot Study of Sequential ("First Strike, Second Strike") Therapies, Modeled on Evolutionary Dynamics of Anthropocene Extinctions, for Hormone Positive Metastatic Breast Cancer
    Condition: Breast
    Intervention: Abemaciclib (); DS-8201a (Trastuzumab Deruxtecan); Faslodex (fulvestrant); LEE011 (Ribociclib); LY2835219 (Abemaciclib); Ribociclib (); Sacituzumab Govitecan (); Taxotere (docetaxel); Trastuzumab Deruxtecan (); Xeloda (capecitabine); capecitabine (); cyclophosphamide (); cytoxan (cyclophosphamide); docetaxel (); fulvestrant ()

    CLINICAL TRIAL 22706
    A Phase 1b/2 Open-Label Study of Disitamab Vedotin Monotherapy or in Combination with Other Anticancer Therapies in Solid Tumors
    Condition: Breast
    Intervention: Disitamab Vedotin (); Tucatinib ()

    CLINICAL TRIAL 23142
    Precision DC: Personalized Neoantigen Dendritic Cell Vaccine Pilot Trial for High Risk Triple Negative Breast Cancer after Neoadjuvant Therapy
    Condition: Breast
    Intervention: DC1 Vaccine ()

    CLINICAL TRIAL 23161
    Immunologic Targeting of Native and Mutated ESR1 Receptor for Treatment of Hormone Receptor Expressing Metastatic Breast Cancer
    Condition: Breast
    Intervention: DC1 Vaccine (); Elacestrant ()

    CLINICAL TRIAL 23179
    Creation of an Infrastructure to Support Delivery of mHealth Interventions for Cancer Patients Throughout Florida
    Condition: Multiple
    Intervention:

    CLINICAL TRIAL 23249
    PRE-I-SPY TRIAL - PRE-Investigation of Serial Studies to Predict Your Therapeutic Response with Imaging And moLecular Analysis: A Phase I/Ib platform trial
    Condition: Breast
    Intervention: ALX148 (); Cemiplimab (); REGN2810 (Cemiplimab); T-Dxd (); Tucatinib (); Vidutolimod (); Zanidatamab ()

    CLINICAL TRIAL 23250
    Randomized phase 2 clinical trial of nab-paclitaxel + durvalumab (MEDI4736) + tremelimumab + neoantigen vaccine vs. nab-paclitaxel + durvalumab (MEDI4736) + tremelimumab in patients with metastatic triple negative breast cancer
    Condition: Breast
    Intervention: AMP-514 (Durvalumab); CP-675,206 (tremelimumab); Durvalumab (); Gemzar (gemcitabine); MEDI4736 (Durvalumab); Nab-paclitaxel (Abraxane); Neoantigen (); Paraplatin (carboplatin); Sacituzumab Govitecan (); carboplatin (); gemcitabine (); tremelimumab ()

    CLINICAL TRIAL 23255
    An Open-Label, Multicenter Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of XL309 (ISM3091) as Single-Agent and Combination Therapy in Patients with Advanced Solid Tumors
    Condition: Multiple
    Intervention: Olaparib (Lynparza); XL309 ()

    CLINICAL TRIAL 23340
    A Phase 2 study of alisertib in combination with endocrine therapy in patients with HR+, HER2-negative recurrent or metastatic breast cancer
    Condition: Breast
    Intervention: Alisertib (MLN8237); Anastrozole (); Arimadex (Anastrozole); Aromasin (Exemestane); Exemestane (); Faslodex (fulvestrant); Femara (Letrozole); Letrozole (); Tamoxifen (); fulvestrant ()

    CLINICAL TRIAL 23366
    Patient-Reported Outcomes in Recipients of Intralesional Vaccines for Breast Cancer at Moffitt Cancer Center
    Condition: Breast
    Intervention:

    CLINICAL TRIAL 23367
    First-in-Human, Escalating Oral Dose Study of RGT-419B Given Alone and with Endocrine Therapy in Subjects with Hormone Receptor Positive, Human Epidermal Growth Factor Receptor 2 Negative Advanced/Metastatic Breast Cancer
    Condition: Breast
    Intervention: RGT419B ()

    CLINICAL TRIAL 23378
    A phase 1/2, first-in-human study to assess the safety, tolerability, pharmacokinetics, pharmacodynamics, and anti-tumor activity of AVZO-021 as a single agent and in combination therapy in patients with advanced solid tumors
    Condition: Breast
    Intervention: 772256 (Palbociclib); AVZO-021 (); Abemaciclib (); Faslodex (fulvestrant); Femara (Letrozole); LEE011 (Ribociclib); LY2835219 (Abemaciclib); Letrozole (); Palbociclib (); Paraplatin (carboplatin); Ribociclib (); Sacituzumab Govitecan (); carboplatin (); fulvestrant ()

    CLINICAL TRIAL 23393
    A Phase 2, Open-Label Study of PCS6422 with Capecitabine in Patients with Advanced or Metastatic Breast Cancer
    Condition: Breast
    Intervention: PCS6422 (); Xeloda (capecitabine); capecitabine ()

    CLINICAL TRIAL 23426
    MammaPrint, BluePrint, and Full-genome Data Linked with Clinical Data to Evaluate New Gene EXpression Profiles: An Adaptable Registry (FLEX Study)
    Condition: Breast
    Intervention: Not Applicable ()

    CLINICAL TRIAL 23433
    Phase II Study of Systemic Screening in Pathologic Node Positive Breast Cancer following Neoadjuvant Chemotherapy and Surgery
    Condition: Breast
    Intervention:

    CLINICAL TRIAL 23480
    A Phase 1/2 Study of a Selective FGFR2/3 Inhibitor, CGT4859, in Patients With Cholangiocarcinoma and Other Advanced Solid Tumors Harboring FGFR2 and/or FGFR3 Genetic Alterations
    Condition: Multiple
    Intervention: CGT4859 ()

    CLINICAL TRIAL 23521
    High Intensity Interval Training: Optimizing Exercise Therapy to Mitigate Cardiovascular Disease Risk Following Breast Cancer Chemotherapy
    Condition: Breast
    Intervention:

    CLINICAL TRIAL 23549
    A Phase 1/1b Study of VET3-TGI Administered Alone and in Combination with Atezolizumab in Patients with Advanced Solid Tumors
    Condition: Thoracic
    Intervention: Atezolizumab (Tecentriq); VET3-TGI ()

    CLINICAL TRIAL 23585
    A Phase 1a/1b Open-Label Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Efficacy of BBO-10203 in Subjects with Advanced Solid Tumors (The BREAKER-101 Trial)
    Condition: Breast
    Intervention: Avastin (Bevacizumab); BBO-10203 (); Bevacizumab (); FOLFOX (); Faslodex (fulvestrant); Herceptin (Trastuzumab); LEE011 (Ribociclib); Ribociclib (); Trastuzumab (); fulvestrant (); rhuMAb HER2 (Trastuzumab)

    CLINICAL TRIAL 23513
    Assessing the DCIS Test Effect on Treatment Strategies in Patients with Ductal Carcinoma in Situ After Breast-Conserving Surgery
    Condition: Breast
    Intervention:

    CLINICAL TRIAL 23572
    Elacestrant versus Standard Endocrine Therapy in Women and Men with Node-positive, Estrogen Receptor-positive, HER2-negative, Early Breast Cancer with High Risk of Recurrence A Global, Multicenter, Randomized, Open-label Phase 3 Study (ELEGANT)
    Condition: Breast
    Intervention: Anastrozole (); Arimadex (Anastrozole); Aromasin (Exemestane); Elacestrant (); Exemestane (); Femara (Letrozole); Letrozole (); Tamoxifen ()

    CLINICAL TRIAL 23553
    DENALI-1: A Seamless Phase 1/2 Study to Evaluate the Safety and Efficacy of A2B395, an Allogeneic Logic-gated Tmod CAR T, in Heterozygous HLA A*02 Adults with Recurrent Unresectable, Locally Advanced, or Metastatic Solid Tumors That Express EGFR and Have Lost HLA A*02 Expression.
    Condition: Immunotherapy
    Intervention: A2B395 (); MESNA (); cyclophosphamide (); cytoxan (cyclophosphamide); fludarabine (Fludarabine phosphate)

    CLINICAL TRIAL 23559
    Aging, DNA Methylation, and Incident Cardiovascular Disease in Breast Cancer Survivors
    Condition: Breast
    Intervention:

    CLINICAL TRIAL 23571
    The MIND-BC Study: MIND Diet for Breast Cancer Cognition
    Condition: Breast
    Intervention:

    CLINICAL TRIAL 23678
    DCIS: RECAST Trial Ductal Carcinoma In Situ: Re-Evaluating Conditions for Active Surveillance Suitability as Treatment: a breast cancer prevention pilot study
    Condition: Breast
    Intervention: Anastrozole (); Arimadex (Anastrozole); Aromasin (Exemestane); Elacestrant (); Exemestane (); Femara (Letrozole); Letrozole (); Tamoxifen (); Testosterone + Anastrozole (); Z-endoxifen ()

    CLINICAL TRIAL 23697
    A Phase 1/1b, Open-label, Multicenter, First-in-human Dose Escalation and Dose Expansion Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Anti-tumor Activity of VVD-159642, a RAS-PI3KA Inhibitor, as a Single Agent and in Combination in Participants With Advanced Solid Tumors
    Condition: Multiple
    Intervention: AMG 510 (Sotorasib); GSK1120212 (Trametinib); Olomorasib (); Sotorasib (); Trametinib (); VVD-159642 ()

    CLINICAL TRIAL 23719
    A Phase III, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study Evaluating the Efficacy and Safety of Inavolisib Plus a CDK4/6 Inhibitor and Letrozole Versus Placebo Plus a CDK4/6 Inhibitor and Letrozole in Patients with Endocrine-Sensitive PIK3CA-Mutated, Hormone Receptor-Positive, HER2-Negative Advanced Breast Cancer
    Condition: Breast
    Intervention: 772256 (Palbociclib); Femara (Letrozole); Inavolisib/Placebo (); Letrozole (); Palbociclib ()

    CLINICAL TRIAL 23766
    A First-in-Human Phase 1 Dose Escalation Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of FID-022 as Monotherapy in Patients with Advanced Solid Tumors
    Condition: Multiple
    Intervention: FID-022 ()