Biotech | Pharma Company | Type/Product Area | Amount | Terms/Details (Month) |
Company** | (Symbol/Country) | |||
(Country) | ||||
I. MODIFIED AGREEMENTS | ||||
Advanced Tissue | Smith & Nephew | Expansion of 4/96 joint | ND | This joint venture was expanded |
Sciences Inc. | plc (U.K.) | venture to commercial- | once in 1/98 to include Derma- | |
ize Dermagraft (for | graft-TC for all wound care appli- | |||
diabetic foot ulcers and | cations outside the U.S. and all | |||
venous and pressure | non-burn wound care applications | |||
ulcers) and Dermagraft- | in U.S.; now, Smith & Nephew | |||
TC (for full and partial- | will market Dermagraft-TC (to be | |||
thickness burns) to | renamed TransCyte) for burns in | |||
include new territory | the U.S. (8/98) | |||
Affymetrix Inc. | American Home | Exercise of option to | ND | American Home exercised option |
Products Corp. | subscribe to Affymetrix's | under 1/98 agreement between its | ||
(NYSE:AHP) | Easy Access program | subsidiary Genetics Institute and | ||
for GeneChip expression | Affymetrix; American Home and | |||
probe arrays | its affiliates get broad access to | |||
custom and standard GeneChips | ||||
plus instrumentation and software; | ||||
Affymetrix gets subscription fees | ||||
and fixed per-chip fees (9/98) | ||||
ArQule Inc. | Amersham Pharma- | Extension of joint | ND | This is the 4th extension; further |
cia Biotech | collaboration to develop | details ND (8/98) | ||
advanced separations | ||||
products, especially | ||||
affinity ligands via | ||||
ArQule's combinatorial | ||||
chemistry; agreement | ||||
dates from 3/95 | ||||
Aurora | Parke-Davis | Expansion of 9/97 | $9M | Wyeth-Ayerst will pay $9M over |
Biosciences Corp. | (division of Warner- | agreement on Aurora's | 15 months for the new system | |
Lambert Co.; NYSE: | ultra-high-throughput | (8/98) | ||
WLA) | screening system | |||
(UHTSS) to include | ||||
development of auto- | ||||
mated master com- | ||||
pound storage system | ||||
for long-term housing | ||||
of chemical and bio- | ||||
logical compounds | ||||
Cell Therapeutics | Ortho Biotech Inc./ | Restructuring of 11/96 | ND | Due to negative results of 1st |
Inc. | The R.W. Johnson | R&D and marketing | Phase III trial, the regulatory time- | |
Pharmaceutical | agreement on lisofylline | line for this drug has been altered; | ||
Research Institute | (anti-inflammatory drug | Cell Therapeutics will now con- | ||
(both are affiliates | for reducing toxicities | trol and fund product development; | ||
of Johnson & John- | from radiation and | Johnson & Johnson will pay its | ||
son; NYSE:JNJ) | chemotherapy in cancer | share through 12/31/98; if new | ||
patients) | Phase III trial is positive, Johnson | |||
& Johnson has option of resuming | ||||
responsibility for product develop- | ||||
ment and marketing; if it exercises | ||||
option, Cell Therapeutics gets | ||||
additional payments; if not, then | ||||
Cell Therapeutics can license prod- | ||||
uct to other 3rd parties (7/98) | ||||
Cima Labs Inc. | Novartis Consumer | Novartis exercised | ND | ND (7/98) |
Health Inc. (division | option under 12/97 | |||
of Novartis AG; | agreement to license | |||
Switzerland) | consumer products | |||
developed via OraSolv | ||||
fast-dissolve technology | ||||
Corixa Corp. | Pasteur Merieux | Extension of 3/97 | ND | This collaboration was already |
Connaught (unit | research agreement and | extended with new options in 1/98, | ||
of Rhone-Poulenc | license option on use | but those options were to expire; | ||
Group; France) | of Corixa's protein | Pasteur Merieux extended its | ||
adjuvant LeIF (Leish- | options until 12/31/98 to license | |||
mania elongation | LeIF exclusively for use in influ- | |||
initiation factor) in | enza and respiratory syncytial | |||
vaccines for infectious | virus vaccines and nonexclusively | |||
diseases | for use in HIV, tuberculosis and | |||
malaria vaccines (8/98) | ||||
SmithKline Beech- | Extension of 10/95 | ND | SmithKline will provide additional | |
am Biologicals SA | collaboration on T-cell | research funding through 5/99 and | ||
(Belgium; subsid- | active recombinant | gets exclusive option to license | ||
iary of SmithKline | subunit vaccines for | Corixa's tuberculosis antigens for | ||
Beecham plc; | infectious diseases, | use as vaccine through 8/99; if it | ||
NYSE:SBH; U.K.) | specifically tuberculosis | exercises option, Corixa gets fee | ||
plus milestones; SmithKline gets | ||||
exclusive worldwide rights except in | ||||
Japan, where Corixa gets co-exclu- | ||||
sive rights (8/98) | ||||
Desmos Inc.* | Baxter Healthcare | Renewal and extension | ND | ND (7/98) |
Corp. (subsidiary of | of 9/97 collaboration on | |||
Baxter International | use of Desmos' extra- | |||
Inc.; NYSE:BAX) | cellular matrix as bio- | |||
coating for percutaneous | ||||
implants used in renal | ||||
therapy | ||||
GeneMedicine Inc. | Corange Interna- | Expansion of 7/95 | ND | Research term of collaboration |
tional Ltd. (unit of | collaboration on non- | extended until 2/02; companies will | ||
Roche Holdings | viral gene therapies for | work exclusively together on gene | ||
Ltd.; Switzerland) | certain cancers to cover | therapies using the 3 genes; focus | ||
all human cancer indica- | on Phase II trial of IL-2 in head and | |||
tions for gene medicines | neck cancer and preclinical through | |||
using genes for interleu- | Phase I/II trials of other 2 genes (same | |||
kin-2 (IL-2), interferon- | indication); on successful completion | |||
alpha (IFN-a) and inter- | of 1 clinical trial, GeneMedicine has | |||
leukin-12 (IL-12); genes | option to share development costs | |||
used alone or in com- | in exchange for 50% of profits or to get | |||
bination | royalties on worldwide sales; Roche | |||
will convert additional equity pay- | ||||
ments under 7/95 agreement into | ||||
research and milestone payments; | ||||
GeneMedicine can partner with other | ||||
firms in gene therapy for cancer using | ||||
different genes (8/98) | ||||
Genzyme | Eli Lilly and Co. | Expansion of 3/98 | $22M | Lilly's option to license protein |
Transgenics Corp. | (NYSE:LLY) | feasibility agreement to | expires 12/99; until then, Genzyme | |
produce a transgenic | Transgenics will get $1M develop- | |||
therapeutic protein | ment funding; on execution of | |||
option, Genzyme Transgenics gets | ||||
funding and milestones of $22M; | ||||
Lilly gets worldwide rights; Gen- | ||||
zyme Transgenics will manufacture | ||||
protein and gets royalties (7/98) | ||||
Hybridon Inc. | G.D. Searle & Co. | Extension and expan- | ND | Searle will continue to support |
(OTC Bulletin | (subsidiary of Mon- | sion of 1/96 collabor- | research through 1/00; Searle has | |
Board:HYBN) | santo Co.; NYSE: | ation on antisense drugs | option of designating additional | |
MTC) | for inflammatory disease | molecular targets; companies also | ||
to include more targets | initiated program focused on onco- | |||
in cardiovascular disease | gene MDM2 (inhibits apoptosis) | |||
and cancer, including | (7/98) | |||
MDM2 oncogene | ||||
Immunex Corp. | American Home | Restructuring of prod- | ND | Immunex no longer obligated to fund |
Products Corp. | uct rights agreements | certain oncology R&D at American | ||
(NYSE:AHP) | and termination of | Home's subsidiary American Cyanamid; | ||
oncology agreement; | Immunex gets worldwide rights to | |||
especially concerns | Leukine and 3 drugs still in clinic | |||
Leukine, Mobist (FLT-3 | (to which American Home had held | |||
ligand), IL-15 and | rights outside North America); Immu- | |||
CD40 ligand | nex will pay royalties to American | |||
Home on ex-North American sales; | ||||
American Home has option to acquire | ||||
rights to 4 future Immunex products; | ||||
Immunex can convert 2 of those calls | ||||
and then pay American Home mile- | ||||
stones and royalties; for exercised | ||||
call, Immunex gets fees, milestones | ||||
and royalties (7/98) | ||||
Incyte | Novartis AG | Expansion of 6/97 | ND | This is the 2nd expansion of the |
Pharmaceuticals | (Switzerland) | database partnership to | partnership; Novartis gets data | |
Inc. | include Incyte's gene | from DNA microarrays from the | ||
expression microarray | UniGEM product line as well as | |||
technology | data from custom microarrays; | |||
Incyte gets access fees and per- | ||||
experiment fees (7/98) | ||||
Pharmacopeia Inc. | Berlex Laboratories | Expansion of 2/95 | ND | Pharmacopeia will get additional |
Inc. (subsidiary of | agreement on use of | research funding, milestones and | ||
Schering AG; | combinatorial chemistry | royalties (8/98) | ||
Germany) | and high-throughput | |||
screening for drug leads | ||||
for multiple sclerosis | ||||
to pursue chemical | ||||
optimization of lead | ||||
compound against | ||||
additional target | ||||
Organon NV | Expansion of 5/96 | ND | Pharmacopeia will get additional | |
(the Netherlands) | agreement on use of | research funding, milestones and | ||
combinatorial chemistry | royalties (8/98) | |||
and high-throughput | ||||
screening for drug leads | ||||
to include development | ||||
of compound against | ||||
additional target | ||||
Phytera Inc.* | Tsumura & Co. | Extension and expansion | ND | Collaboration extended through |
(Japan) | of 6/96 collaboration | 6/00; Phytera gets research funds | ||
on use of Phyton's plant | and milestones; companies co-own | |||
cell culture extract librar- | products; Phytera gets exclusive | |||
ies to screen for small mole- | rights in North America; Tsumura | |||
cules to treat rheumatoid | gets exclusive rights elsewhere; | |||
arthritis and allergies; will | companies will pay each other | |||
now also screen Phytera's | royalties (8/98) | |||
marine microorganism | ||||
extract libraries | ||||
Regeneron | Sumitomo Pharma- | Expansion of 6/94 col- | $5M | Sumitomo licensed the product |
Pharmaceuticals | ceuticals Co. Ltd. | laboration on BDNF | for developing in Japan; Regeneron | |
Inc. | (Japan) | (brain-derived neuro- | gets initial $5M payment plus | |
trophic factor) for | milestones and royalties (8/98) | |||
treating amyotrophic | ||||
lateral sclerosis | ||||
II. TERMINATED AGREEMENTS | ||||
Cambridge | Boehringer Ingel- | Termination of 1/95 | — | Based on further evaluation of |
NeuroScience Inc. | heim International | collaboration on Cere- | negative Phase III interim results, | |
GmbH (Germany) | stat (NMDA ion- | companies have terminated collab- | ||
channel blocker) for | oration but are still negotiating | |||
traumatic brain | specific terms and conditions (7/98) | |||
injury and stroke | ||||
CoCensys Inc. | G.D. Searle & Co. | Termination of 5/96 | — | Searle ended agreement but pro- |
(subsidiary of Mon- | collaboration on | vided no explanation; CoCensys | ||
santo Co.; NYSE: | CCD 3693 (synthetic | retains all rights to compounds in | ||
MTC) | epalon or neuroactive | this program (7/98) | ||
steroid) for treating | ||||
insomnia (Phase I | ||||
trials completed) | ||||
Corvas | Schering-Plough | Termination of 12/94 | — | Companies terminated this pro- |
International Inc. | Corp. (NYSE:SGP) | collaboration on orally | gram after disappointing results of | |
bioavailable thrombin | a Phase I trial; the 2 other research | |||
inhibitors for prevent- | programs (on inhibitors of Factor | |||
ing and treating cardio- | Xa and hepatitis C virus) remain | |||
vascular disorders | intact (8/98) | |||
Diatide Inc. | Nycomed Amer- | Termination of 8/95 | — | Nycomed will discontinue R&D |
sham plc (U.K.) | option and develop- | payments for early-stage products | ||
ment agreement on | as of 1/31/99; Diatide regains U.S. | |||
early-stage imaging | rights to all non-optioned products; | |||
products | decision does not affect license | |||
and co-promotion agreements on | ||||
AcuTect and P829 imaging prod- | ||||
ucts (8/98) | ||||
Gilead Sciences | Glaxo Wellcome | Termination of 7/90 | — | The companies jointly decided to |
Inc. | plc (NYSE:GLX; | collaboration on genetic | end this collaboration (under a | |
U.K.) | code blockers (including | 3/96 extension, Glaxo had option | ||
antisense and triple- | to terminate after 2 years); each | |||
helix compounds) | company retains rights to jointly | |||
developed technology as well as | ||||
its own research results (6/98) | ||||
MorphoSys | Pharmacia & | Termination of 3/97 | — | Pharmacia & Upjohn made stra- |
GmbH* | Upjohn Inc. | research collaboration | tegic decision to focus its research | |
(Germany) | (NYSE:PNU; | on use of MorphoSys' | in areas other than inflammation; | |
U.K.) | human antibody library | plans to continue into 2nd phase of | ||
and phage-based screen- | collaboration were suspended | |||
ing technology to iden- | (8/98) | |||
tify lead compounds and | ||||
therapeutic targets for | ||||
inflammation and other | ||||
diseases | ||||
Ophidian | Eli Lilly and Co. | Termination of 5/96 | — | Lilly said it will discontinue pro- |
Pharmaceuticals | (NYSE:LLY) | collaboration on avian | gram; Ophidian regains all rights | |
Inc. | polyclonal antibody to | to product (9/98) | ||
neutralize toxins | ||||
secreted by Clostridium | ||||
difficile (gastrointes- | ||||
tinal infection; Phase I | ||||
trial completed) | ||||
Neurogen Corp. | Schering-Plough | Conclusion of joint | — | Schering-Plough moved the re- |
Corp. (NYSE:SGP) | research phase of 6/95 | search in-house; if drug candidates | ||
collaboration on small-mol- | progress through clinic, Neurogen | |||
ecule drugs that modulate | gets milestones and royalties; | |||
dopamine receptor sub- | Neurogen retains option to manu- | |||
types for treating | facture products for U.S. market | |||
schizophrenia | (7/98) | |||
NOTES: | ||||
# This chart contains information on modified and terminated agreements only, covering the time period between 6/16/98 and 9/21/98. It does not include arrangements that are classed strictly as production, marketing and/or distribution agreements, nor does it include any collaborations that involve agricultural product development. | ||||
For a chart listing new collaborations between big pharma and biotech companies for the same time period (6/16/98 - 9/21/98), see the 9/28/98 issue of BioWorld Financial Watch. | ||||
ND = Not disclosed, reported and/or available | ||||
* Private companies are indicated with an asterisk. | ||||
** Unless otherwise noted, the trading symbols for public biotechnology companies can be found by referring to the BioWorld Stock Report For Public Biotechnology Companies on pp. 13-14. |