MedPath

ImmunoGen, Inc.

ImmunoGen, Inc. logo
🇺🇸United States
Ownership
Public, Subsidiary
Established
1981-01-01
Employees
501
Market Cap
-
Website
http://www.immunogen.com

Clinical Trials

44

Active:27
Completed:14

Trial Phases

3 Phases

Phase 1:40
Phase 2:1
Phase 3:3

Drug Approvals

2

NMPA:1
FDA:1

Drug Approvals

Mirvetuximab Soravtansine Injection

Product Name
爱拉赫
Approval Number
国药准字SJ20240044
Approval Date
Nov 22, 2024
NMPA

Clinical Trials

Distribution across different clinical trial phases (44 trials with phase data)• Click on a phase to view related trials

Phase 1
40 (90.9%)
Phase 3
3 (6.8%)
Phase 2
1 (2.3%)

First-in-Human Study of IMGC936 in Participants With Advanced Solid Tumors

Phase 1
Completed
Conditions
Advanced Solid Tumor
Interventions
First Posted Date
2020-11-10
Last Posted Date
2025-01-15
Lead Sponsor
ImmunoGen, Inc.
Target Recruit Count
56
Registration Number
NCT04622774
Locations
🇺🇸

UCSD, La Jolla, California, United States

🇺🇸

Sarah Cannon Research Institute, Denver, Colorado, United States

🇺🇸

Florida Cancer Specialists, Sarasota, Florida, United States

and more 10 locations

A Study of Mirvetuximab Soravtansine in Platinum-Resistant, Advanced High-Grade Epithelial Ovarian, Primary Peritoneal, or Fallopian Tube Cancers With High Folate Receptor-Alpha Expression

Phase 3
Completed
Conditions
Peritoneal Cancer
Epithelial Ovarian Cancer
Fallopian Tube Cancer
Interventions
First Posted Date
2020-03-05
Last Posted Date
2024-08-07
Lead Sponsor
ImmunoGen, Inc.
Target Recruit Count
106
Registration Number
NCT04296890
Locations
🇺🇸

Arizona Oncology Associates, Phoenix, Arizona, United States

🇺🇸

City of Hope Medical Center, Duarte, California, United States

🇺🇸

California Cancer Associates (cCARE), Fresno, California, United States

and more 86 locations

Open-label Study of IMGN779 in Adult Patients With Relapsed/Refractory CD33-positive Acute Myeloid Leukemia

Phase 1
Completed
Conditions
Acute Myeloid Leukemia
Interventions
First Posted Date
2016-02-04
Last Posted Date
2019-09-04
Lead Sponsor
ImmunoGen, Inc.
Target Recruit Count
62
Registration Number
NCT02674763
Locations
🇺🇸

Comprehensive Cancer Center (UAB CCC), Birmingham, Alabama, United States

🇺🇸

Dana-Farber Cancer Institute, Boston, Massachusetts, United States

🇺🇸

New Mexico Cancer Care Alliance, Albuquerque, New Mexico, United States

and more 4 locations

A Study of Mirvetuximab Soravtansine vs. Investigator's Choice of Chemotherapy in Women With Folate Receptor (FR) Alpha Positive Advanced Epithelial Ovarian Cancer (EOC), Primary Peritoneal or Fallopian Tube Cancer

Phase 3
Completed
Conditions
Epithelial Ovarian Cancer
Primary Peritoneal Carcinoma
Fallopian Tube Cancer
Ovarian Cancer
Interventions
First Posted Date
2015-12-16
Last Posted Date
2020-10-14
Lead Sponsor
ImmunoGen, Inc.
Target Recruit Count
366
Registration Number
NCT02631876
Locations
🇺🇸

University of Alabama at Birmingham, Birmingham, Alabama, United States

🇺🇸

Arizona Oncology Associates, PC - HAL, Tempe, Arizona, United States

🇺🇸

Arizona Oncology Associates, PC - HOPE, Tucson, Arizona, United States

and more 128 locations

Study of Mirvetuximab Soravtansine in Combination With Bevacizumab, Carboplatin, Pegylated Liposomal Doxorubicin, Pembrolizumab, or Bevacizumab + Carboplatin in Participants With Folate Receptor Alpha (FRα) Positive Advanced Epithelial Ovarian Cancer, Primary Peritoneal, or Fallopian Tube Cancer

Phase 1
Completed
Conditions
Epithelial Ovarian Cancer
Primary Peritoneal Cancer
Fallopian Tube Cancer
Interventions
First Posted Date
2015-11-17
Last Posted Date
2024-06-14
Lead Sponsor
ImmunoGen, Inc.
Target Recruit Count
264
Registration Number
NCT02606305
Locations
🇺🇸

University of California at Los Angeles, Los Angeles, California, United States

🇺🇸

Massachusetts General Hospital, Boston, Massachusetts, United States

🇺🇸

Dana-Farber Cancer Institute, Boston, Massachusetts, United States

and more 9 locations
  • Prev
  • 1
  • 2
  • 3
  • 4
  • Next

News

Crescent Biopharma Appoints Jan Pinkas as Chief Scientific Officer to Advance Oncology Pipeline

Crescent Biopharma has appointed Jan Pinkas, Ph.D., as chief scientific officer, bringing over two decades of oncology drug development experience including expertise in antibody-drug conjugates.

Oxford BioTherapeutics and Boehringer Ingelheim Advance Third Oncology Drug Candidate to IND-Enabling Studies

Oxford BioTherapeutics announced that Boehringer Ingelheim has selected a third drug candidate targeting OB33 to advance into IND-enabling studies under their ongoing collaboration.

Day One Biopharmaceuticals Appoints Michael Vasconcelles as Head of R&D to Drive Pipeline Expansion

Day One Biopharmaceuticals has appointed Michael Vasconcelles, M.D., as Head of Research and Development, bringing over 25 years of oncology research and development expertise to the company.

Pharmaceutical Industry Sees Wave of Board Appointments as Companies Strengthen Leadership

Pharmaceutical and biotech companies across Europe and North America have made significant board appointments, bringing industry veterans and scientific experts to strengthen their leadership teams.

CytomX's CX-2051 Shows Promising 28% Response Rate in Advanced Colorectal Cancer Phase 1 Trial

CytomX's EpCAM-targeting antibody-drug conjugate CX-2051 demonstrated a 28% confirmed response rate in late-line colorectal cancer patients, significantly outperforming current standard therapies with single-digit response rates.

Cantargia's Novel Anti-IL1RAP Antibody-Drug Conjugate Shows Promising Preclinical Efficacy Against Cancer

Cantargia's anti-IL1RAP antibody-drug conjugate demonstrated potent anti-tumor activity across different IL1RAP expression levels in preclinical models, with a single dose achieving 100% survival in high-expressing tumors.

Federal Circuit Ruling on ImmunoGen's Dosing Patent Highlights Challenges in Pharmaceutical Patent Strategy

The Federal Circuit has affirmed that ImmunoGen's patent application for a specific dosing regimen of mirvetuximab soravtansine (IMGN853) was obvious, despite the inventors' claim of solving an unknown ocular toxicity problem.

Elahere Receives European Commission Approval for Platinum-Resistant Ovarian Cancer

The European Commission has granted marketing authorization to AbbVie's Elahere for treating folate receptor-alpha (FRα) positive, platinum-resistant ovarian cancer.

EU Approves AbbVie's Elahere for Platinum-Resistant Ovarian Cancer

AbbVie's Elahere (mirvetuximab soravtansine) receives EU approval for folate receptor-alpha (FRα) positive, platinum-resistant ovarian cancer, marking a significant advancement in treatment options.

European Commission Approves AbbVie's Elahere for Folate Receptor-Alpha Positive Ovarian Cancer

The European Commission has approved AbbVie's Elahere for treating folate receptor-alpha (FRα) positive, platinum-resistant ovarian cancer in adults after one to three prior systemic treatments.

© Copyright 2025. All Rights Reserved by MedPath