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Last $5.95 USD
Change Today +0.02 / 0.34%
Volume 145.4K
CERU On Other Exchanges
As of 8:10 PM 05/29/15 All times are local (Market data is delayed by at least 15 minutes).

cerulean pharma inc (CERU) Snapshot

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03/19/15 - $10.87
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08/5/14 - $3.35
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cerulean pharma inc (CERU) Details

Cerulean Pharma Inc., a clinical-stage company, develops nanopharmaceutical product candidates in the areas of oncology and other diseases in the United States. The company’s lead product candidate is CRLX101, a tumor targeted nanoparticle-drug conjugate (NDC), which is in Phase II clinical trials for the treatment of relapsed renal cell carcinoma and relapsed ovarian cancer; and in Phase Ib clinical trials for the treatment of neoadjuvant rectal cancer, as well as in Phase II clinical trials for other indications, such as gastric cancer and small cell lung cancer. It is also developing CRLX301, a platform-generated clinical candidate, which is in Phase I clinical development for the treatment of tumor-targeted NDC. The company was formerly known as Tempo Pharmaceuticals, Inc. and changed its name to Cerulean Pharma Inc. in October 2008. Cerulean Pharma Inc. was incorporated in 2005 and is based in Cambridge, Massachusetts.

39 Employees
Last Reported Date: 04/7/15
Founded in 2005

cerulean pharma inc (CERU) Top Compensated Officers

Chief Executive Officer, President and Direct...
Total Annual Compensation: $432.6K
Senior Vice President of Finance & Administra...
Total Annual Compensation: $301.9K
Chief Medical Officer and Senior Vice Preside...
Total Annual Compensation: $407.9K
Compensation as of Fiscal Year 2014.

cerulean pharma inc (CERU) Key Developments

Cerulean Pharma Inc., Q1 2015 Earnings Call, May 06, 2015

Cerulean Pharma Inc., Q1 2015 Earnings Call, May 06, 2015

Cerulean Announces Fast Track Designation Granted for CRLX101 in Metastatic Renal Cell Carcinoma

Cerulean Pharma Inc. announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation to Cerulean’s lead nanoparticle-drug conjugate, CRLX101, in combination with Avastin® (bevacizumab) for the treatment of metastatic renal cell carcinoma (mRCC) following progression through two or three prior lines of therapy. The FDA’s Fast Track Program is designed to facilitate the development and expedite the review of drugs that are intended to treat serious conditions and fulfill an unmet medical need. CRLX101 is currently being evaluated in combination with Avastin as a treatment of relapsed renal cell carcinoma in a randomized Phase 2 trial. CRLX101 is a dynamically tumor-targeted nanoparticle-drug conjugate (NDC) designed to concentrate in tumors and slowly release its anti-cancer payload, camptothecin, inside tumor cells. CRLX101 inhibits topoisomerase 1 (topo 1), which is involved in cellular replication, and hypoxia-inducible factor-1a (HIF-1a), which research suggests is a master regulator of cancer cell survival mechanisms thought to promote drug and radiation resistance. CRLX101 has shown activity in four different tumor types, both as monotherapy and in combination with other cancer treatments. CRLX101 is currently in Phase 2 clinical development and has been dosed in more than 250 patients and has Fast Track designation in combination with Avastin® in metastatic renal cell carcinoma.

Cerulean Pharma Inc. Presents at UBS Global Healthcare Conference, May-19-2015 09:00 AM

Cerulean Pharma Inc. Presents at UBS Global Healthcare Conference, May-19-2015 09:00 AM. Venue: Sheraton New York Times Square Hotel, 811 Seventh Avenue, New York, New York, United States. Speakers: Christopher D.T. Guiffre, Chief Executive Officer, President and Director.


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Price/Sales 3,669.3x
Price/Book 3.0x
Price/Cash Flow NM Not Meaningful
TEV/Sales 2,776.1x

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