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CRESCENT BIOPHARMA, INC. (CBIO)

Crescent Biopharma, Inc. is a biotechnology firm dedicated to the research and development of novel cancer therapies. Its investigational portfolio notably includes CR-001, a proprietary bispecific antibody engineered to simultaneously target PD-1 and VEGF pathways for the treatment of solid tumors. The company's pipeline further comprises CR-002 and CR-003. Crescent Biopharma also maintains a strategic alliance with Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd., focusing on the joint advancement and commercialization of oncology therapeutics, encompassing innovative combination approaches. The company's operations are headquartered in Waltham, Massachusetts.

Sector: Pharmaceutical Preparations

Industry: Biotechnology

Crescent Biopharma, Inc. logo

Crescent Biopharma, Inc.

NASDAQ:CBIOHealthcare
-4.19%$13.48
AH$13.67+1.41%vs close
Mkt Cap$500.74M
Float20.86M
O/S37.15M
Vol
$ Vol
RVOL
Inst Own79.5%
SI21.2%
Earnings
Dilution
Phase Distribution
19 lead-sponsored trials·1 active·14 completed
Phase 112
Phase 1/24
Phase 21
Phase 32
(5 more as collaborator)
Status Overview
Recruiting1
Completed14
Stopped4

Trials need funding. See this company's dilution risk and cash position.

Clinical Trials
Sponsor role
Status
Phase
  • Phase 3
    Terminated

    Safety of Rivipansel (GMI-1070) in the Treatment of One or More Vaso-Occlusive Crises in Hospitalized Subjects With Sickle Cell Disease

    Rivipansel

    Sickle Cell Anemia, Sickle Cell Disease +3

    Enrollment
    154
    Start
    Dec 2015
    Primary Completion
    Nov 2019
    Completion
    Nov 2019
    NCT02433158
  • Phase 3
    Terminated

    Study to Determine the Efficacy of Uproleselan (GMI-1271) in Combination With Chemotherapy to Treat Relapsed/Refractory Acute Myeloid Leukemia

    Uproleselan, Placebo

    Acute Myeloid Leukemia

    Enrollment
    388
    Start
    Oct 2018
    Primary Completion
    Mar 2024
    Completion
    Mar 2024
    NCT03616470
  • Phase 2
    Completed

    Study of GMI-1070 for the Treatment of Sickle Cell Pain Crisis

    GMI-1070, Placebo

    Sickle Cell Disease, Vaso-occlusive Crisis +1

    Enrollment
    81
    Start
    May 2010
    Primary Completion
    Dec 2012
    Completion
    Dec 2013
    NCT01119833
  • Phase 1/2
    Completed

    Study of Intravenous GMI-1070 in Adults With Sickle Cell Disease

    GMI-1070

    Sickle Cell Disease

    Enrollment
    15
    Start
    May 2009
    Primary Completion
    Jul 2010
    Completion
    Sep 2010
    NCT00911495
  • Phase 1/2
    Completed

    Study to Determine Safety, Pharmacokinetics and Efficacy of GMI-1271 in Combination With Chemotherapy in AML

    GMI-1271, Mitoxantrone

    Leukemia, Myeloid, Acute

    Enrollment
    91
    Start
    Mar 2015
    Primary Completion
    Dec 2017
    Completion
    May 2018
    NCT02306291
  • Phase 1/2
    Terminated

    Study to Assess Safety, Tolerability, and Efficacy of GMI-1271 in Patients With Calf-level Deep Venous Thrombosis (DVT)

    GMI-1271, Enoxaparin Sodium (Lovenox®)

    Deep Venous Thrombosis

    Enrollment
    2
    Start
    Jul 2016
    Primary Completion
    Nov 2016
    Completion
    Nov 2016
    NCT02744833
  • Phase 1/2
    Recruiting

    CR-001 in Adult Participants With Locally Advanced or Metastatic Solid Tumors

    CR-001, Paclitaxel

    Locally Advanced / Metastatic Solid Tumors

    Enrollment
    540
    Start
    Feb 2026
    Primary Completion
    Feb 2029est.
    Completion
    Feb 2029est.
    NCT07335497
  • Phase 1
    Completed

    A Study to Evaluate the Effect of IV Doses of GMI-1070 on Qtc Intervals in Healthy African-American Adult Subjects

    Rivipansel

    Healthy

    Enrollment
    48
    Start
    Aug 2013
    Primary Completion
    Aug 2014
    Completion
    Aug 2014
    NCT01941511
  • Phase 1
    Completed

    Placebo-controlled Single Dose Study to Evaluate Safety and Pharmacokinetics of GMI-1271 in Healthy Volunteers

    GMI-1271, Placebo

    Healthy Adult Subjects

    Enrollment
    28
    Start
    Jun 2014
    Primary Completion
    Aug 2014
    Completion
    Apr 2015
    NCT02168595
  • Phase 1
    Completed

    Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Subcutaneous Rivipansel With rHuPH20 in Healthy Subjects

    Rivipansel, Placebo

    Healthy

    Enrollment
    27
    Start
    Oct 2015
    Primary Completion
    Apr 2016
    Completion
    Apr 2016
    NCT02217917
  • Phase 1
    Completed

    Phase I Study to Assess Safety and Pharmacokinetics of GMI-1271 in Healthy Adult Subjects

    GMI-1271, Placebo

    Healthy Volunteers

    Enrollment
    32
    Start
    Oct 2014
    Primary Completion
    Mar 2016
    Completion
    Mar 2016
    NCT02271113
  • Phase 1
    Completed

    A Study to Evaluate the PK, Safety and Tolerability of GMI-1271 With and Without Filgrastim in Healthy Adult Subjects

    GMI-1271, Filgrastim

    Healthy Volunteers

    Enrollment
    54
    Start
    Nov 2015
    Primary Completion
    Aug 2016
    Completion
    Aug 2016
    NCT02703051
  • Phase 1
    Completed

    A Study to Determine the Efficacy, Safety and Pharmacokinetics of GMI-1271 as Adjunct to Standard of Care for the Treatment of Multiple Myeloma

    GMI-1271

    Multiple Myeloma

    Enrollment
    10
    Start
    Jun 2016
    Primary Completion
    Apr 2019
    Completion
    Apr 2019
    NCT02811822
  • Phase 1
    Completed

    A Study to Evaluate the Effect of IV Doses of Rivipansel on Subjects With Renal Impairment and in Healthy Subjects

    Rivipansel

    Renal Impairment, Healthy

    Enrollment
    28
    Start
    Jun 2016
    Primary Completion
    Feb 2018
    Completion
    Feb 2018
    NCT02813798
  • Phase 1
    Completed

    A Study to Evaluate the Effect of IV Doses of Rivipansel in Subjects With Moderate Hepatic Impairment and in Healthy Subjects With Normal Hepatic Function

    Rivipansel

    Moderate Hepatic Impairment, Normal Hepatic Function

    Enrollment
    16
    Start
    Sep 2016
    Primary Completion
    Feb 2017
    Completion
    Mar 2017
    NCT02871570
  • Phase 1
    Completed

    Placebo-Controlled Single Dose Study to Evaluate Safety and Pharmacokinetics of GMI-1359 in Healthy Volunteers

    GMI-1359, Placebo

    Healthy

    Enrollment
    58
    Start
    Aug 2016
    Primary Completion
    Oct 2017
    Completion
    Nov 2018
    NCT02931214
  • Phase 1
    Completed

    A Study to Evaluate the Effect of Age on the Pharmacokinetics, Safety and Tolerability of IV Rivipansel.

    Rivipansel

    Healthy

    Enrollment
    16
    Start
    Jan 2017
    Primary Completion
    Feb 2017
    Completion
    Mar 2017
    NCT02998099
  • Phase 1
    Completed

    A Study in Healthy Volunteers to Investigate How Much Test Medicine [14C]-Uproleselan is Taken up by the Body When Administered Directly Into the Vein (IV)

    Uproleselan

    Healthy Subjects

    Enrollment
    5
    Start
    Aug 2018
    Primary Completion
    Sep 2018
    Completion
    Sep 2018
    NCT03606447
  • Phase 1
    Terminated

    A Study to Determine Safety and Tolerability of GMI-1359 in Subjects With HR+ Metastatic Breast Cancer

    GMI-1359

    HR+ Metastatic Breast Cancer, Breast Cancer +1

    Enrollment
    4
    Start
    Nov 2019
    Primary Completion
    Aug 2021
    Completion
    Aug 2021
    NCT04197999