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248    MANAGING KNOWLEDGE WORK AND INNOVATION

                          still not agree on what might be causing the formation of particles. The clinical trials
                          team were very keen to establish this as soon as possible as they kept repeating that
                          every day ‘saved’ in development was potentially worth $1million but the same sense
                          of urgency was not manifest in the chemists. Suggestions were made to delve further
                          into the published literature, ask others (possibly academics) to become involved but
                          this was going to take a lot of time. Eventually two of the three chemists that were
                          present at the project team meeting decided on a way forward, counter to what had
                          been proposed by another chemist, and went away ‘to solve the problem quickly and
                          internally’. At the time the study ended at BIOTECH, the 123–3 trial was way behind
                          schedule and reluctantly a decision had been made to inform the partner. There was
                          uncertainty regarding how Stallion would react to this news.


                          >> PARTNERING PROCESS
                          BIOTECH has started to assess interest in 2006 from a limited number of potential
                          licensees (all large pharmaceutical firms), with a final decision on the choice of partner
                          scheduled for early 2008. Those who expressed an interest were given an information
                          pack developed by the project team specifically about the project. The project team
                          had significant involvement in supporting partnering negotiations but knew noth-
                          ing of the financial details surrounding the negotiations. A shortlist of four potential
                          partners had been identified and future clinical trials development plans had been
                          soliticited from each by the BIOTECH Business Development team. These plans were
                          discussed around three key areas: (i) whether the plans indicated that the partner
                          had appropriate expertise to take the product to market efficiently; (ii) whether the
                          plans gave any clues to BIOTECH about whether or not to start particular clinical tri-
                          als in advance of partnering being agreed; (iii) what questions the BIOTECH Business
                          Development team should seek potential partners to answer helping them decide on
                          the final partnering agreement. In this way BIOTECH was conducting a form of due
                          diligence (see ‘Glossary of terms’) on potential partners.
                            Clinical team recommendations for future trials were also presented to the Devel-
                          opment Project Team (DPT – see section on ‘Knowledge share and project manage-
                          ment’) in November 2006. There was significant debate around which proposed trials
                          to fund on the basis of future partnering. The major problem facing the project at
                          this point in the development process then was managing the tensions that arise in
                          clinical trial design whilst simultaneously identifying a partner. Even after the part-
                          ner had been identified in early 2007, negotiations regarding the precise terms of
                          the agreement could continue for another 9–12 months. The clinical team spent a
                          significant amount of their time ‘guessing’ what potential partners might require when
                          attempting to decide on whether or not to go ahead with proposed future trials. This
                          was made more difficult by the fact that there was no clear consensus amongst the
                          partners about what kind of studies should be done. The DPT had explicitly instructed
                          the clinical team to suggest what would be crucial to the partnering deal but ‘with our
                          knowledge of partners we can’t say hand on heart what will be critical’ (Clinical Trials
                          Manager). Moreover the knowledge of partners also appeared to be limited – ‘part-
                          ners don’t necessarily know what trials they need’ and ‘any partner is going to stop









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                  9780230_522015_11_cha10.indd   248                                         6/5/09   7:21:37 AM
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