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 | $111M | Companies signed binding letter |
Sciences Inc. | plc (U.K.) | joint venture to com- | (equity; | of intent to expand joint venture; |
mercialize Dermagraft | % ND) | Advanced Tissue gets $35M over | ||
for treating diabetic | next 12 months for additional | |||
foot ulcers to include | indications, including immediate | |||
indications of venous | $20M in equity purchase, $16M | |||
and pressure ulcers as | in milestones and 1-time payment | |||
well as commercial- | of $10M for demonstrating ability | |||
ization of Dermagraft- | of Dermagraft-TC for treating | |||
TC for treating burns | pressure sores (1/98) | |||
Allelix Biophar- | Eli Lilly Canada | Expansion of 1989 | ND | Expansion will increase Lilly's |
maceuticals Inc. | Inc. (unit of Eli | basic research collab- | total investment in Allelix to | |
(Canada) | Lilly and Co.; | oration to apply new | more than US$21M since partner- | |
NYSE:LLY) | technologies to 2 drug | ship began; collaboration already | ||
discovery programs | extended once in 1/95 (1/98) | |||
(excitatory amino acid | ||||
receptors as targets for | ||||
drugs to treat central | ||||
nervous system dis- | ||||
orders; neuropeptide Y | ||||
receptor as target for | ||||
drugs to treat eating | ||||
disorders) | ||||
Alza Corp. | Janssen Pharma- | Expansion of agreement | $21.5M | Alza will make 1-time payment of |
ceutica Inc. | to develop an E-Trans | $21.5M to Janssen and will share | ||
(Belgium; unit of | fentanyl product for | operating profits from U.S. sales | ||
Johnson & John- | treating acute pain | and get royalties on sales else- | ||
son; NYSE:JNJ) | (currently in Phase III | where; Janssen has right to market | ||
trials; uses electric cur- | product and Alza has right to co- | |||
rent to control drug | promote in U.S. (1/98) | |||
administration through | ||||
skin) | ||||
Aurora | Eli Lilly and Co. | Aurora provided | ND | Aurora and Lilly signed a collab- |
Biosciences | (NYSE:LLY) | Lilly with a sublicense | oration in 1/97 giving Lilly | |
Corp. and Sibia | to Sibia's transcription- | access to Aurora's technologies | ||
Neurosciences | based functional bio- | for use in its internal drug discov- | ||
Inc. | assay for drug screening, | ery program; Aurora and Sibia | ||
to be used in conjunc- | cross-licensed each other's drug | |||
tion with Aurora's fluor- | screening technologies in 1/97 and | |||
escent assay technol- | Aurora has now granted Lilly a | |||
ogies and other drug | sublicense; Sibia got up-front pay- | |||
screening services | ment, annual maintenance fees and | |||
royalties (1/98) | ||||
Aurora | Merck & Co. Inc. | Aurora provided | ND | Aurora and Merck signed a collab- |
Biosciences | (NYSE:MRK) | Merck with a sub- | oration in 12/97 giving Merck | |
Corp. and Sibia | license to Sibia's | access to Aurora's technologies | ||
Neurosciences | patent on high-through- | for use in its internal drug discov- | ||
Inc. | put drug screening, for | ery program; Aurora and Sibia | ||
use in conjunction | cross-licensed each other's drug | |||
with Aurora's fluor- | screening technologies in 1/97 and | |||
escent assay technol- | Aurora now has granted Merck a | |||
ogies and other drug | sublicense; Sibia got up-front pay- | |||
screening services | ment (1/98) | |||
Connetics Corp. | Soltec Research | Connetics exercised its | ND | Connetics gets exclusive rights to |
Pty Ltd. | option under 6/96 agree- | develop and market product in | ||
(Australia) | ment to license clobeta- | North America (1/98) | ||
sol mousse for treating | ||||
severe dermatoses (high- | ||||
potency corticosteroid | ||||
formulated as quick- | ||||
break foam) | ||||
Corixa Corp. | Pasteur Merieux | Extension and expan- | ND | Relationship stems from prior |
Connaught (unit | sion of 3/97 collabora- | option agreement for Pasteur Mer- | ||
of Rhone-Poulenc | tion on use of Corixa's | ieux to license exclusive rights to | ||
Group; France) | protein adjuvant LeIF | LeIF as adjuvant; now, Pasteur | ||
(Leishmanial eukaryotic | Merieux has received new option | |||
initiation factor) in | to commercialize LeIF in same | |||
vaccines for infectious | disease areas as previously; this | |||
diseases; expanded to | option expires 6/30/98 (1/98) | |||
include comparisons of | ||||
LeIF to other adjuvants | ||||
SmithKline | Extension of Smith- | $2M | As part of 3/97 cancer vaccine | |
Beecham Biologic- | Kline's option under | collaboration, Corixa granted | ||
als SA (Belgium; | 3/97 cancer vaccine | SmithKline 2 options for licensing | ||
unit of SmithKline | agreement to license | its programs for vaccine develop- | ||
Beecham plc; | early-stage antigen | ment; SmithKline paid $2M to | ||
NYSE:SBH; U.K.) | discovery program for an | extend the 1st option until 9/30/99 | ||
undisclosed cancer target | (the 2nd option must be acted on | |||
by 3Q:98) (2/98) | ||||
Cytel Corp. | Nextran unit of | Expansion and exten- | ND | New agreement allows for broader |
Baxter Healthcare | sion of 10/96 collab- | application of Cytel's carbohy- | ||
Corp. (NYSE:BAX) | oration on Cytel's alpha | drate products (made via sugar | ||
galactose carbohydrate | nucleotide cycling technology); | |||
product for use in anti- | Cytel has exclusive agreement to | |||
transplant rejection | supply products to Nextran; Cytel | |||
device to include other | gets milestones; Baxter invested | |||
carbohydrate products | $1M in Cytel's $8.4M private | |||
for treating rejection | placement (12/97); Cytel will | |||
associated with xeno- | develop and manufacture products | |||
transplantation | (2/98) | |||
Emisphere | Eli Lilly and Co. | Expansion of 2/97 | ND | Lilly executed 2 license agree- |
Technologies | (NYSE:LLY) | agreement to use | ments and made 2 milestone pay- | |
Inc. | Emisphere's technology | ments to Emisphere (both are part | ||
for oral delivery of | of the terms of the original agree- | |||
therapeutic proteins and | ment) (3/98) | |||
exercise of 2 options to | ||||
license technology for | ||||
2 specific Lilly proteins | ||||
(1 in osteoporosis; 1 in | ||||
endocrinology, including | ||||
growth disorders) | ||||
Epimmune Inc. | G.D. Searle & Co. | Definitive agreement | $100M | Letter of intent signed 9/97, at |
(subsidiary of | (wholly owned sub- | to collaborate on cancer | (13.4% | which time Searle invested $5M |
Cytel Inc.) | sidiary of Monsanto | vaccines developed via | equity) | in Cytel; in definitive agreement, |
Co.; NYSE:MTC) | Epimmune's library of | Searle invested additional $3.9M | ||
antigenic cancer epitopes | in Cytel preferred stock and $6.1M | |||
and immunostimulant | in Epimmune preferred stock; | |||
technology (PADRE) | Cytel simultaneously invested | |||
$3.9M in Epimmune preferred | ||||
stock; Searle now owns 13.4% of | ||||
Epimmune, while Cytel owns the | ||||
rest; preclinical and clinical mile- | ||||
stones could total $100M over | ||||
next 10-12 years; Searle gets world- | ||||
wide exclusive rights to Epimmune's | ||||
epitope and PADRE technologies | ||||
in cancer field (excluding rights | ||||
previously granted elsewhere); | ||||
Epimmune gets royalties (3/98) | ||||
Genome | Schering-Plough | Extension of 12/95 | $7M | Collaboration extended through |
Therapeutics | Corp. (NYSE:SGP) | collaboration on anti- | 3/31/00; guaranteed payments to | |
Corp. | infective agents for drug- | Genome Therapeutics raised from | ||
resistant bacteria, includ- | $13M to $20M (it can also get as | |||
ing Staphylococcus | much as $23.5M more in mile- | |||
aureus, via Genome | stones) (3/98) | |||
Therapeutics' genomics- | ||||
based high-throughput | ||||
screening, target vali- | ||||
dation and assay | ||||
development | ||||
Human Genome | Takeda Chemical | Takeda exercised option | ND | Takeda exercised its option to |
Sciences Inc. | Industries Ltd. | under 6/95 agreement | develop and commercialize pro- | |
(Japan) | to license Human Ge- | duct in Japan; Human Genome | ||
nome's genomics-derived | got option fee for these rights and | |||
product candidate mye- | will get milestones and royalties; | |||
loid progenitor inhibitory | further details ND (2/98) | |||
factor-1 (currently in U.S. | ||||
Phase I trials for protecting | ||||
hematopoietic progenitor | ||||
cells from effects of | ||||
chemotherapy) | ||||
Incyte | Novartis AG | Expansion of 6/97 | ND | Novartis gets nonexclusive access |
Pharmaceuticals | (Switzerland) | database partnership | to LifeSeq database in exchange | |
Inc. | to include Incyte's | for annual access fees; further | ||
LifeSeq gene sequence | details ND (1/98) | |||
and expression database | ||||
Pfizer Inc. | Extension and expan- | ND | Pfizer will continue to have access | |
(NYSE:PFE) | sion of 6/94 genomic | to Incyte's databases, including | ||
database partnership to | its LifeSeq gene sequence and | |||
include LifeSeq FL data- | expression database as well as | |||
base of full-length genes | others; collaboration extended for | |||
and LifeSeq GeneAlbum | 3 years (intent announced 12/97); | |||
DNA clone set | financial details ND (2/98) | |||
LeukoSite Inc. | Warner-Lambert | Extension of 11/96 | ND | Two-year extension of collabora- |
Co. (NYSE:WLA) | collaboration on small | tion (already expanded once in | ||
molecule antagonists to | 11/97) (1/98) | |||
the CCR5 and CXCR4 | ||||
receptors (chemokine | ||||
coreceptors used by | ||||
HIV to enter T cells) | ||||
Ligand | Eli Lilly and Co. | Extension of Ligand's | $20M | Lilly extended Ligand's option so |
Pharmaceuticals | (NYSE:LLY) | option (under 11/97 | that Ligand has additional time to | |
Inc. | alliance on meta- | complete its evaluation and asses- | ||
bolic diseases) to | ment of product; if Ligand exer- | |||
acquire selected rights | cises option, Lilly gets milestones | |||
to 1 of Lilly's specialty | of $20M in Ligand stock; if Ligand | |||
drugs in certain mar- | does not exercise option, it can | |||
kets of interest to | elect to sell $20M in equity to | |||
Ligand | Lilly at 20% premium to market | |||
(3/98) | ||||
SmithKline | Expansion of 2/95 | ND | The collaboration was expanded | |
Beecham plc | collaboration on small | twice; in 2/97, SmithKline exer- | ||
(NYSE:SBH; U.K.) | molecule, orally available | cised its option to include a 3rd | ||
drugs to control hemato- | drug discovery target and bought | |||
poiesis; use of Ligand's | $2.5M in Ligand stock; in 8/97, | |||
STAT technology (signal | SmithKline extended the term of | |||
transducers and activators | the collaboration and bought a | |||
of transcription) to target | $2.5M convertible note (although | |||
hematopoietic growth | both these events occurred in 1997, | |||
factors | Ligand announced them in 1998) | |||
(3/98) | ||||
MedImmune Inc. | SmithKline | Finalized agreement | $85M | Agreement, proposed 12/97, was |
Beecham plc | (from 12/97) to develop | subject to clearance under anti- | ||
(NYSE:SBH; U.K.) | human papillomavirus | trust laws, which occurred (1/98) | ||
(HPV) vaccines for pre- | ||||
venting cervical cancer | ||||
and genital warts | ||||
Onyx | Parke-Davis | Extension of 5/95 | $25M | Collaboration extended for 3 years; |
Pharmaceuticals | (division of | collaboration on drugs | Onyx gets $25M in committed | |
Inc. | Warner-Lambert Co.; | that affect cell-cycle | funding plus milestones; Warner- | |
NYSE:WLA) | regulation; for treat- | Lambert also gets marketing rights | ||
ing cancer and hyper- | in Japan (as well as rest of world); | |||
proliferative diseases | Onyx gets milestones tied specifi- | |||
cally to development efforts in | ||||
Japan (1/98) | ||||
OSI Pharma- | Wyeth-Ayerst | Exercise of option to | ND | Wyeth-Ayerst gets exclusive |
ceuticals Inc. | Laboratories | license series of small | worldwide license to compounds; | |
(division of Ameri- | molecule, gene-transcrip- | further details ND (1/98) | ||
can Home Products | tion-based compounds | |||
Corp.; NYSE:AHP) | that modulate expression | |||
of phosphoenol pyruvate | ||||
carboxykinase (PEPCK) for | ||||
treating Type II diabetes | ||||
Repligen Corp. | Glaxo Wellcome | Extension of 11/94 | ND | One-year extension; Glaxo will use |
plc (NYSE:GLX; U.K.) | collaboration on chemo- | assay to screen its internal com- | ||
kine inhibitors; com- | pound library; Repligen will | |||
panies have jointly | supply Glaxo with 1 of its carbo- | |||
developed high-through- | hydrate analogue combinatorial | |||
put screening assay to | libraries for screening, too; Glaxo | |||
identify small molecules | gets worldwide rights to any prod- | |||
that block interaction of | ucts; Repligen gets research sup- | |||
pro-inflammatory chemo- | port and royalties; Glaxo has | |||
kine with its receptor | option to acquire rights to active | |||
compounds from Repligen's | ||||
library (1/98) | ||||
Ribozyme | Parke-Davis | Definitive agreement | ND | Letter of intent signed 12/97; |
Pharmaceuticals | (division of | on collaboration to | Ribozyme Pharmaceuticals will | |
Inc. | Warner-Lambert Co.; | evaluate specific disease- | design and synthesize ribozymes | |
NYSE:WLA) | related genes for drug | against target genes designated by | ||
intervention using | Parke-Davis; financial terms ND | |||
Ribozyme's target val- | (3/98) | |||
idation technology | ||||
(involves use of ribo- | ||||
zymes to discover gene | ||||
function and validate | ||||
gene targets) | ||||
Trega | Ono Pharmaceutical | Letter of intent to | ND | Ono will fund additional research |
Biosciences Inc. | Co. Ltd. (Japan) | expand 6/97 collabor- | and pay milestones and royalties; | |
ation on orally active | Trega will optimize and screen | |||
small molecules for | lead compounds discovered by | |||
treating diseases medi- | Ono in new area of interest; other | |||
ated by melanocortin | details ND (2/98) | |||
receptor (i.e., inflam- | ||||
matory diseases) to | ||||
include a new target of | ||||
interest to Ono | ||||
Vimrx | Baxter Healthcare | Official naming of new | $130M | Companies signed letter of intent |
Pharmaceuticals | Corp. (subsidiary of | cell therapy company | (equity; | to form the new company (which |
Inc. | Baxter International | Nexell Therapeutics | % ND) | is 80% owned by Vimrx and 20% |
Inc.; NYSE:BAX) | Inc. (formed in 1997 | owned by Baxter) in 6/97; the | ||
to develop cell therapies | definitive agreement was signed in | |||
for cancer and other | 10/97 and Vimrx shareholders | |||
diseases by combining | approved the deal in 12/97; Baxter | |||
Baxter's ex vivo cellular | and Vimrx together contributed | |||
selection and storage | $40M to fund Nexell; Baxter is | |||
business with Vimrx's | responsible for manufacturing, | |||
access to gene therapy | sales, marketing and distribution | |||
and genomics technology) | of products; Nexell will focus on | |||
R&D, partnerships and marketing | ||||
development (2/98) | ||||
II. TERMINATED AGREEMENTS | ||||
Amylin | Johnson & Johnson | Termination of 6/95 | — | Johnson & Johnson provided 6 |
Pharmaceuticals | (NYSE:JNJ) | collaboration on Pram- | months' notice of its intent to | |
Inc. | lintide (synthetic ana- | terminate the collaboration, saying | ||
logue of human hormone | it was no longer in its best inter- | |||
amylin) for treating | ests; all product rights return to | |||
Types I and II diabetes | Amylin, which will restructure its | |||
(currently in Phase III | operations and reduce workforce | |||
trials) | by 25% so it can continue product | |||
development (3/98) | ||||
Anergen Inc. | Novo Nordisk A/S | Termination of 8/93 | — | This collaboration was extended |
(NYSE:NVO; | collaboration on use of | for 2 years in 4/96, but Novo has | ||
Denmark) | AnergiX technology | now terminated it, as part of its | ||
(inactivates disease- | change in strategic direction; all | |||
related T cells) for | product rights return to Anergen; | |||
various diseases, includ- | Novo will reimburse Anergen for | |||
ing multiple sclerosis | cost of ongoing clinical trial; Aner- | |||
(Phase I trial ongoing) | gen has no future obligations to | |||
Novo; Anergen will restructure its | ||||
operations and reduce workforce | ||||
(2/98) | ||||
Immusol Inc.* | Pfizer Inc. | Conclusion of 3/95 | — | Partnership will not be renewed; |
(NYSE:PFE) | collaboration to | Pfizer will fund program through | ||
develop ribozyme gene | 5/98, after which Immusol will | |||
therapy for treating | continue product development | |||
HIV infection (program | (HIV gene therapy currently in | |||
was part of Pfizer's | Phase I trials) (3/98) | |||
R&D initiative | ||||
Pfizergen) | ||||
NaPro | Baker Norton | Termination of 1993 | $14.5M | Partners terminated their agree- |
BioTherapeutics | Pharmaceuticals | development and | ment after the FDA ruled in 12/97 | |
Inc. | Inc. (wholly owned | marketing agreement | that Ivax's paclitaxel-based drug | |
subsidiary of Ivax | on paclitaxel (compound | Paxene for treating AIDS-related | ||
Corp.; AMEX:IVX) | extracted from needles | Kaposi's sarcoma might not get | ||
and limb stock of | marketing approval until 8/04; | |||
ornamental yew trees) | Ivax gets royalty-free, nonexclu- | |||
sive license to NaPro's pending | ||||
patents on stable formulation of | ||||
paclitaxel in U.S., Europe and cer- | ||||
tain other markets; NaPro gets | ||||
$6M cash, $6.4M on issuance of | ||||
patents and the return of 1.1M | ||||
shares of its stock ($2.1M) held by | ||||
Ivax; NaPro will supply a certain | ||||
amount of paclitaxel to Ivax (3/98) | ||||
NOTES: | ||||
# This chart contains information on modified and terminated agreements only, covering the time period between 1/1/98 and 3/24/98. 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 (1/1/98 - 3/24/98), see the 3/30/98 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. |