The Record...
Sharon wanted information on licensing. The status of the drug should provide this data. We'll look at the entire record to see if there is anything else that might be of interest.
The first part of the record in Pharmaprojects includes basic drug data, such as the drug name, company information, and synonyms for the drug. Note that there is no separate listing for trade or brand names in this database. All names are listed under synonyms.
This file, like IMS, has extensive market data. It also has extensive status information including the status of each country globally where the drug is being marketed. This should help Sharon track marketing of the drug worldwide.
Note: In order to give you supplemental information (tips, learn more comments) about the Dialog record, we have had to add spaces between some of the fields. Print out the complete record for File 128 to have a concise duplicate of the Dialog record you will retrieve online. You can compare it to the parts of the record we will highlight later in the lesson.
Here are a few things Sharon might want to see from this part of the record.
- Drug/product name: Pharmaprojects compiles a wealth of alternative product nomenclature, including chemical names, lab codes, brand names, and generic names. These facilitate initial identification and provide more synonyms for effective follow-up searches in biomedical literature files. Tip 3-3
- Company name: The company name field includes
the originator and licensee. Pharmaprojects always
prefers parent company names in indexing for both
originators and licensees, but will often include
originating subsidiary names in the text.

- Other parts of the record include the molecular formula and CAS® Registry Number
Tip 3-4 Tip 3-5 - Synonyms: In Pharmaprojects the synonyms field includes the trade or brand name, laboratory code, and generic name, unlike IMS R&D Focus which provides separate fields for each data element.
- Development status: Pharmaprojects provides thorough recaps of developmental stage transitions and dates and consistently identifies when records were last updated. This file shows the most advanced stage of development a compound has reached in any country.
- Patent information is also provided in
some records. The patent number, country where the
patent was filed, and priority information (date
the patent was first filed and country of filing).
The patent assignee is not listed as it was in IMS.

Review the bibliographic parts of the record and then go to the next page.
1/19/1
DIALOG(R)File 128: PHARMAPROJECTS
(c) 2007 INFORMA UK LTD. All rights reserved.
0030985 ** Image available **
Drug Name: vatalanib
World Status: Phase III Clinical Trial
Pharma Status: Active
Synonyms: CGP-79787
CGP-79787D
PTK-787
PTK/ZK
VEGF-TK1
ZK-222584
Originator: Novartis (Switzerland) [Phase III Clinical Trial]
New Entity: Yes
Latest Upd: Updated On By Latest Change
20070119 JB Filing plans updated
CHEMICAL DATA
Origin: Code Description
CH-SY Chemical, synthetic
Tip 3-6 Tip 3-7
CAS Reg. No: 212141-54-3
Rot. Bonds: 4
Mol. Formula: C20H15CLN4
Hydrogen Bond Donors: 1 Hydrogen Bond Acceptors: 4
Mol. Weight: 346.82 AlogP: 4.46
Chemical Name:
N-(4-Chlorophenyl)-4-(pyridin-4-ylmethyl)phthalazin-1-amine
Tip 3-8
STRUCTURE
COUNTRY DATA
Status: (Active)
France Phase II Clinical Trial/Licensing
Availability Unknown
Germany Phase III Clinical Trial/Licensing
Availability Unknown
Switzerland Phase III Clinical Trial/Licensing
Availability Unknown
World Phase III Clinical Trial
*Portions of record not shown.
We can see from the Status information that vatalanib has reached Phase III Clinical Trial in Germany and Switzerland, but is still in Phase II Clinical Trials in France.
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