Columbia Laboratories Events Calendar 

Archived Events

 Event Date  Replay Until 
Event: Advisory Committee for Reproductive Health Drugs of the FDA review of NDA 22-139, progesterone gel 8% for the proposed indication of "reduction of risk of preterm birth in women with short uterine cervical length regardless of other risk factors in the mid-trimester of pregnancy.” 01/20/2012
TBD by CDER
CBRX to Present at Lazard Capital Markets Healthcare Conference 11/15/2011 01/15/2012
CBRX Q3 2011 Financial Results Conference Call 11/03/2011 11/03/2012
CBRX Q2 2011 Financial Results Conference Call 08/04/2011 08/04/2012
CBRX Q1 2011 Financial Results Conference Call  05/05/2011 05/05/2012
CBRX Q4 2010 Financial Results Conference Call 03/10/2011 03/10/2012

 

The previously-recorded webcasts included in this "Events" section are provided as a service to investors and other interested parties. They contain forward-looking statements, which statements are indicated by the words “may,” “will,” “plans,” “believes,” “expects,” “anticipates,” “potential,” “should,” and similar expressions. Such forward-looking statements involve known and unknown risks, uncertainties, and other factors that may cause actual results to differ materially from those projected in the forward-looking statements. Readers are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date on which they were made. Factors that might cause future results to differ include, but are not limited to, the following: the successful marketing of CRINONE® by Watson Pharmaceuticals, Inc., in the United States and by Merck Serono outside the United States; successful development of a next-generation vaginal progesterone product; success in timely filing and obtaining acceptance of the regulatory filings for and approval of new products and new indications for current products by the United States Food and Drug Administration (FDA) and international regulatory agencies, the outcome of further analyses by the FDA of the clinical data in the Preterm Birth NDA; success in obtaining timely approval of the Preterm Birth NDA by the FDA; the timing and level of success of a future product launch, if any; difficulties or delays in manufacturing; the availability and pricing of third party sourced products and materials; changes in the laws and regulations, including Medicaid; successful compliance with FDA and other governmental regulations applicable to manufacturing facilities, products and/or businesses; the ability to obtain and enforce patents and other intellectual property rights;the impact of competitive products and pricing; the timely and successful negotiation of partnerships or other transactions; the strength of the United States dollar relative to international currencies, particularly the euro; competitive economic and regulatory factors in the pharmaceutical and healthcare industry; general economic conditions; and other risks and uncertainties that may be detailed, from time-to-time, in Columbia's reports filed with the SEC. Columbia does not undertake any responsibility to revise or update any forward-looking statements contained herein.