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Last $18.02 USD
Change Today +0.12 / 0.67%
Volume 962.0K
IMGN On Other Exchanges
Symbol
Exchange
NASDAQ GS
As of 8:10 PM 07/31/15 All times are local (Market data is delayed by at least 15 minutes).

immunogen inc (IMGN) Snapshot

Open
$16.97
Previous Close
$17.90
Day High
$18.78
Day Low
$16.80
52 Week High
07/17/15 - $19.43
52 Week Low
12/23/14 - $5.34
Market Cap
1.6B
Average Volume 10 Days
891.7K
EPS TTM
$-0.70
Shares Outstanding
86.2M
EX-Date
--
P/E TM
--
Dividend
--
Dividend Yield
--
Current Stock Chart for IMMUNOGEN INC (IMGN)

immunogen inc (IMGN) Related Businessweek News

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immunogen inc (IMGN) Details

ImmunoGen, Inc., a biotechnology company, develops targeted anticancer therapeutics. It develops its products using its antibody-drug conjugates technology. The company offers Kadcyla, an antibody-drug conjugate for the treatment of HER2-positive metastatic breast cancer. Its product candidates include IMGN853, which is in Phase I clinical trials for the treatment of ovarian cancer, endometrial cancer, and other cancers; IMGN289 that is in Phase I clinical trials for treating squamous cell carcinoma of head and neck cancer, and non-small cell lung cancer; IMGN529, which is in Phase I clinical trials for the treatment of non-Hodgkin lymphoma and chronic lymphocytic leukemia; and IMGN779 that is in preclinical stage for treating acute myeloid leukemia. The company also develops compounds, such as AMG 172 that is in Phase I clinical trials for the treatment of clear cell renal cell carcinoma; AMG 595, which is in Phase I clinical trials for treating glioblastoma; BAY 94-9343 is in early clinical trials for the treatment of mesothelioma and ovarian cancer; BT-062 for multiple myeloma; SAR3419, which has completed Phase II clinical trials for the treatment of diffuse large B-cell lymphoma; SAR650984 that is in early clinical trials for the treatment of multiple myeloma; SAR566658 that is in Phase I clinical trials for treating CA6-positive solid tumors; and SAR408701 for solid tumors. It has collaborations with Amgen Inc.; Bayer HealthCare; Biotest AG; Eli Lilly and Company; Novartis Institutes for BioMedical Research, Inc.; the Roche Group; and Sanofi. The company was founded in 1981 and is headquartered in Waltham, Massachusetts.

immunogen inc (IMGN) Top Compensated Officers

Chief Executive Officer, President and Direct...
Total Annual Compensation: $544.5K
Chief Financial Officer and Executive Vice Pr...
Total Annual Compensation: $245.0K
Chief Development Officer and Executive Vice ...
Total Annual Compensation: $432.4K
Executive Vice President of Distinguished Res...
Total Annual Compensation: $377.2K
Compensation as of Fiscal Year 2014.

immunogen inc (IMGN) Key Developments

Immunogen, Inc. Releases CD37-Targeting ADC, IMGN529

ImmunoGen, Inc. announced the first presentation of findings with the company’s CD37-targeting ADC, IMGN529, in combination with the CD20-targeting antibody, rituximab (Rituxan), in preclinical assessments. These data are being presented in a poster at the 13thInternational Conference on Malignant Lymphoma taking place in Lugano, Switzerland. Among the findings being presented are: IMGN529 exhibits strong synergy with rituximab and other CD20-targeting antibodies in cell lines representative of an array of non-Hodgkin lymphoma (NHL) subtypes, including both GCB and ABC diffuse large B-cell lymphoma (DLBCL); Consistent with the in vitro findings, the combination of IMGN529 and rituximab was highly active against DLBCL models in vivo; Synergy also was seen in vitro in amodel representative of “double hit” lymphoma, a particularly difficult-to-treat type of DLBCL characterized by deregulation of two different genes, BCL2 (or BCL6) and MYC; and Both IMGN529’s antibody component and its DM1 payload contributed to its synergistic activity with rituximab.

ImmunoGen, Inc. Announces Data from Phase I Ovarian Cancer Trial

ImmunoGen, Inc. has announced data from a Phase I trial with FRá-targeting antibody-drug conjugate, or ADC, mirvetuximab soravtansine, in patients with platinum-resistant ovarian cancer. The findings reported are from an ongoing Phase I trial. Once the recommended Phase II dose (RP2D) of mirvetuximab soravtansine was established during dose finding, an expansion cohort was opened to assess the safety and activity of this ADC specifically in the treatment of patients with FRá-positive platinum-resistant ovarian cancer. Approximately 80% of the patients screened have met the criteria for having FRá-positive disease. Twenty-two patients were included in the analysis =- two from the dose-escalation phase of the trial and the twenty enrolled in the expansion cohort at the time of data cutoff for presentation. All had FRá-positive platinum-resistant ovarian cancer and had received mirvetuximab soravtansine at the RP2D (6.0 mg/kg, given every three weeks). All had previously received taxane as well as platinum therapy. Thirteen were still on study at the time of data cutoff. The majority of adverse events reported were low grade (grade 1 or 2), with diarrhea, blurred vision, nausea, vomiting, fatigue, and abdominal pain the most common treatment-emergent events reported (> 20% of patients). Seventeen of the 22 patients were included in the efficacy analysis; the other five patients were still on study and had not yet reached their first assessment. Nine of these 17 patients had an objective response (8 partial responses, 1 complete response) to treatment, for an ORR of 53%. The responses in six of these nine patients were ongoing at the time of data cutoff, with five of these six patients on treatment for more than 15 weeks. The findings are from a Phase I trial assessing mirvetuximab soravtansine for the treatment of FRá-positive solid tumors. After the RP2D was established in patients likely to have FRá-positive disease using a once every 3-week dosing schedule, an expansion cohort was opened to evaluate the ADC specifically in patients with FRá-positive platinum-resistant ovarian cancer when administered as a single agent at this RP2D. To be eligible for enrollment in this expansion cohort, patients must have ovarian cancer that responded to primary platinum therapy, but then progressed within six months or progressed on or within six months of treatment with subsequent platinum therapy. The cancer also must be FRá-positive, assessed by immunohistochemistry. Approximately 80% of patients screened met this criteria based on the CLIA lab assay. This expansion cohort has been expanded from 20 to 40 patients to obtain additional experience in this patient population.

ImmunoGen, Inc. Presents at Sachs Immuno-Oncology: BD&L and Investment Forum, May-29-2015 09:50 AM

ImmunoGen, Inc. Presents at Sachs Immuno-Oncology: BD&L and Investment Forum, May-29-2015 09:50 AM. Venue: Hyatt Chicago Magnificent Mile, Chicago, Illinois, United States. Speakers: Richard J. Gregory, Chief Scientific Officer and Executive Vice President of Research.

 

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IMGN

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Valuation IMGN Industry Range
Price/Earnings NM Not Meaningful
Price/Sales 18.3x
Price/Book 44.7x
Price/Cash Flow NM Not Meaningful
TEV/Sales 14.9x
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